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Wyszukujesz frazę ""GONADAL dysgenesis"" wg kryterium: Temat

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Wyświetlanie 61-80 z 2626
Tytuł:
Prenatal detection and molecular cytogenetic characterization of Xp deletion and Xq duplication: a case report and literature review.
Autorzy:
Lin, Qing
Liang, Chunya
Du, Bole
Li, Lijiao
Li, Hong
Mai, Xiaolan
Li, Sheng
Xu, Wenyu
Wu, Cunzhen
Zeng, Mi
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Temat:
LITERATURE reviews
CHROMOSOME abnormalities
GENETIC counseling
X chromosome
CYTOPLASMIC inheritance
GONADAL dysgenesis
Źródło:
BMC Medical Genomics; 2/21/2024, Vol. 17 Issue 1, p1-11, 11p
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Genetic analysis of a pedigree with MECP2 duplication syndrome in China.
Autorzy:
Zeng, Lan
Zhu, Hui
Wang, Jin
Wang, Qiyan
Pang, Ying
Luo, Zemin
Chen, Ai
Qin, Shengfang
Zhu, Shuyao
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Temat:
CHROMOSOME analysis
GENEALOGY
RESPIRATORY infections
GENETIC counseling
PATIENTS' families
GONADAL dysgenesis
Źródło:
BMC Medical Genomics; 2/19/2024, Vol. 17 Issue 1, p1-9, 9p
Terminy geograficzne:
CHINA
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
New NR5A1 mutations and phenotypic variations of gonadal dysgenesis.
Autorzy:
Werner R; Department of Paediatrics and Adolescent Medicine, Division of Experimental Paediatric Endocrinology and Diabetes, University of Lübeck, Lübeck, Germany.
Mönig I; Department of Paediatrics and Adolescent Medicine, Division of Experimental Paediatric Endocrinology and Diabetes, University of Lübeck, Lübeck, Germany.
Lünstedt R; Department of Paediatrics and Adolescent Medicine, Division of Experimental Paediatric Endocrinology and Diabetes, University of Lübeck, Lübeck, Germany.
Wünsch L; Department of Paediatric Surgery, University Hospital of Lübeck, Germany.
Thorns C; Department of Pathology, University Hospital of Lübeck, Lübeck, Germany.
Reiz B; Institute for Cardiogenetics, University of Lübeck, Lübeck, Germany.
Krause A; Department of Paediatrics and Adolescent Medicine, Paediatric Endocrinology and Diabetes, University Hospital Freiburg, Freiburg, Germany.
Schwab KO; Department of Paediatrics and Adolescent Medicine, Paediatric Endocrinology and Diabetes, University Hospital Freiburg, Freiburg, Germany.
Binder G; Department of Paediatrics and Adolescent Medicine, Eberhard-Karls-University of Tübingen, Tübingen, Germany.
Holterhus PM; Division of Paediatric Endocrinology and Diabetes, Department of Paediatrics, Christian-Albrechts-University, Kiel, Germany.
Hiort O; Department of Paediatrics and Adolescent Medicine, Division of Experimental Paediatric Endocrinology and Diabetes, University of Lübeck, Lübeck, Germany.
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Źródło:
PloS one [PLoS One] 2017 May 01; Vol. 12 (5), pp. e0176720. Date of Electronic Publication: 2017 May 01 (Print Publication: 2017).
Typ publikacji:
Case Reports; Journal Article
MeSH Terms:
Mutation*
Gonadal Dysgenesis/*genetics
Gonadal Dysgenesis/*physiopathology
Steroidogenic Factor 1/*genetics
Adolescent ; Child ; Female ; Follow-Up Studies ; Gonadal Dysgenesis/therapy ; HeLa Cells ; Humans ; Male ; Phenotype ; Steroidogenic Factor 1/metabolism ; T-Box Domain Proteins/genetics
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Revisiting the hybridization processes in the Triatoma brasiliensis complex (Hemiptera, Triatominae): Interspecific genomic compatibility point to a possible recent diversification of the species grouped in this monophyletic complex.
Autorzy:
Pinotti H; Laboratório de Parasitologia, Departamento de Ciências Biológicas, Universidade Estadual Paulista 'Júlio de Mesquita Filho' (UNESP), Faculdade de Ciências Farmacêuticas, Araraquara, São Paulo, Brasil.
de Oliveira J; Laboratório de Parasitologia, Departamento de Ciências Biológicas, Universidade Estadual Paulista 'Júlio de Mesquita Filho' (UNESP), Faculdade de Ciências Farmacêuticas, Araraquara, São Paulo, Brasil.
Ravazi A; Instituto de Biociências, Universidade Estadual Paulista 'Júlio de Mesquita Filho', IBB/UNESP, Botucatu, São Paulo, Brasil.
Madeira FF; Laboratório de Biologia Celular, Departamento de Biologia, Instituto de Biociências, Letras e Ciências Exatas, Universidade Estadual Paulista 'Júlio de Mesquita Filho', IBILCE/UNESP, São José do Rio Preto, São Paulo, Brasil.
Dos Reis YV; Instituto de Biociências, Universidade Estadual Paulista 'Júlio de Mesquita Filho', IBB/UNESP, Botucatu, São Paulo, Brasil.
de Oliveira ABB; Laboratório de Biologia Celular, Departamento de Biologia, Instituto de Biociências, Letras e Ciências Exatas, Universidade Estadual Paulista 'Júlio de Mesquita Filho', IBILCE/UNESP, São José do Rio Preto, São Paulo, Brasil.
Azeredo-Oliveira MTV; Laboratório de Biologia Celular, Departamento de Biologia, Instituto de Biociências, Letras e Ciências Exatas, Universidade Estadual Paulista 'Júlio de Mesquita Filho', IBILCE/UNESP, São José do Rio Preto, São Paulo, Brasil.
Rosa JAD; Laboratório de Parasitologia, Departamento de Ciências Biológicas, Universidade Estadual Paulista 'Júlio de Mesquita Filho' (UNESP), Faculdade de Ciências Farmacêuticas, Araraquara, São Paulo, Brasil.
Alevi KCC; Laboratório de Parasitologia, Departamento de Ciências Biológicas, Universidade Estadual Paulista 'Júlio de Mesquita Filho' (UNESP), Faculdade de Ciências Farmacêuticas, Araraquara, São Paulo, Brasil.; Instituto de Biociências, Universidade Estadual Paulista 'Júlio de Mesquita Filho', IBB/UNESP, Botucatu, São Paulo, Brasil.
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Źródło:
PloS one [PLoS One] 2021 Oct 15; Vol. 16 (10), pp. e0257992. Date of Electronic Publication: 2021 Oct 15 (Print Publication: 2021).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Genetic Variation*
Hybridization, Genetic*
Phylogeny*
Chimera/*genetics
Insect Vectors/*genetics
Triatoma/*genetics
Animals ; Chagas Disease/parasitology ; Chagas Disease/transmission ; Chromosomes, Insect/genetics ; Cytogenetic Analysis ; Female ; Gene Flow ; Gonadal Dysgenesis/genetics ; Gonadal Dysgenesis/pathology ; Insect Vectors/classification ; Insect Vectors/parasitology ; Male ; Reproduction/genetics ; Testis/pathology ; Testis/physiopathology ; Triatoma/classification ; Triatoma/parasitology ; Trypanosoma cruzi
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
A homozygous missense variant in HSD17B4 identified in a consanguineous Chinese Han family with type II Perrault syndrome.
Autorzy:
Chen K; Department & Institute of Neurology, Huashan Hospital, Fudan University, 12 Wulumuqi Zhong Road, Shanghai, 200040, China.
Yang K; Department & Institute of Neurology, Huashan Hospital, Fudan University, 12 Wulumuqi Zhong Road, Shanghai, 200040, China.
Luo SS; Department & Institute of Neurology, Huashan Hospital, Fudan University, 12 Wulumuqi Zhong Road, Shanghai, 200040, China.
Chen C; Department & Institute of Neurology, Huashan Hospital, Fudan University, 12 Wulumuqi Zhong Road, Shanghai, 200040, China.
Wang Y; Department & Institute of Neurology, Huashan Hospital, Fudan University, 12 Wulumuqi Zhong Road, Shanghai, 200040, China.
Wang YX; Department & Institute of Neurology, Huashan Hospital, Fudan University, 12 Wulumuqi Zhong Road, Shanghai, 200040, China.
Li DK; Department & Institute of Neurology, Huashan Hospital, Fudan University, 12 Wulumuqi Zhong Road, Shanghai, 200040, China.
Yang YJ; Department & Institute of Neurology, Huashan Hospital, Fudan University, 12 Wulumuqi Zhong Road, Shanghai, 200040, China.
Tang YL; Department & Institute of Neurology, Huashan Hospital, Fudan University, 12 Wulumuqi Zhong Road, Shanghai, 200040, China.
Liu FT; Department & Institute of Neurology, Huashan Hospital, Fudan University, 12 Wulumuqi Zhong Road, Shanghai, 200040, China.
Wang J; Department & Institute of Neurology, Huashan Hospital, Fudan University, 12 Wulumuqi Zhong Road, Shanghai, 200040, China.
Wu JJ; Department & Institute of Neurology, Huashan Hospital, Fudan University, 12 Wulumuqi Zhong Road, Shanghai, 200040, China.
Sun YM; Department & Institute of Neurology, Huashan Hospital, Fudan University, 12 Wulumuqi Zhong Road, Shanghai, 200040, China. .
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Źródło:
BMC medical genetics [BMC Med Genet] 2017 Aug 23; Vol. 18 (1), pp. 91. Date of Electronic Publication: 2017 Aug 23.
Typ publikacji:
Case Reports; Journal Article
MeSH Terms:
Homozygote*
Mutation, Missense*
Asian People/*genetics
Gonadal Dysgenesis, 46,XX/*genetics
Hearing Loss, Sensorineural/*genetics
Peroxisomal Multifunctional Protein-2/*genetics
Adult ; Cell Line ; Female ; Gene Expression Regulation ; Genetic Testing ; Gonadal Dysgenesis, 46,XX/diagnosis ; Hearing Loss, Sensorineural/diagnosis ; Heterozygote ; Humans ; Magnetic Resonance Imaging ; Pedigree ; Peroxisomal Multifunctional Protein-2/metabolism ; Sequence Analysis, DNA
SCR Disease Name:
Gonadal dysgenesis XX type deafness
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Delayed Diagnosis of a 17-Hydroxylase/17,20-Lyase Deficient Patient Presenting as a 46,XY Female: A Low Normal Potassium Level Can Be an Alerting Diagnostic Sign.
Autorzy:
Çamtosun E; Ankara University Faculty of Medicine, Department of Pediatric Endocrinology, Ankara, Turkey, E-mail: .
Şıklar Z
Ceylaner S
Kocaay P
Berberoğlu M
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Źródło:
Journal of clinical research in pediatric endocrinology [J Clin Res Pediatr Endocrinol] 2017 Jun 01; Vol. 9 (2), pp. 163-167. Date of Electronic Publication: 2016 Dec 23.
Typ publikacji:
Case Reports; Journal Article
MeSH Terms:
Delayed Diagnosis*
Gonadal Dysgenesis, 46,XY*
Adrenal Hyperplasia, Congenital/*diagnosis
Potassium/*blood
Steroid 17-alpha-Hydroxylase/*metabolism
Adrenal Hyperplasia, Congenital/blood ; Adrenal Hyperplasia, Congenital/genetics ; Child, Preschool ; Diagnosis, Differential ; Disorders of Sex Development/blood ; Disorders of Sex Development/diagnosis ; Disorders of Sex Development/genetics ; Female ; Follicle Stimulating Hormone/blood ; Humans ; Luteinizing Hormone/blood ; Steroid 17-alpha-Hydroxylase/genetics
SCR Disease Name:
46, XY female
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Unilateral ovarian absence in a Black-headed Squirrel Monkey (Saimiri vanzolinii Ayres, 1985), a threatened neotropical primate species.
Autorzy:
Lopes GP; Laboratory of Amazon Animal Biotechnology and Medicine, Federal University of Pará, Castanhal, PA, Brazil.; Mamirauá Institute for Sustainable Development, Tefé, AM, Brazil.
Brito AB; Laboratory of Amazon Animal Biotechnology and Medicine, Federal University of Pará, Castanhal, PA, Brazil.
Santos RR; Laboratory of Amazon Animal Biotechnology and Medicine, Federal University of Pará, Castanhal, PA, Brazil.
Domingues SFS; Laboratory of Amazon Animal Biotechnology and Medicine, Federal University of Pará, Castanhal, PA, Brazil.
Paim FP; Mamirauá Institute for Sustainable Development, Tefé, AM, Brazil.; Federal University of Minas Gerais, Belo Horizonte, MG, Brazil.
Queiroz HL; Laboratory of Amazon Animal Biotechnology and Medicine, Federal University of Pará, Castanhal, PA, Brazil.; Mamirauá Institute for Sustainable Development, Tefé, AM, Brazil.
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Źródło:
Journal of medical primatology [J Med Primatol] 2017 Jun; Vol. 46 (3), pp. 87-89. Date of Electronic Publication: 2017 Mar 27.
Typ publikacji:
Case Reports; Research Support, Non-U.S. Gov't
MeSH Terms:
Gonadal Dysgenesis/*veterinary
Ovary/*abnormalities
Saimiri/*abnormalities
Animals ; Brazil ; Endangered Species ; Female ; Gonadal Dysgenesis/diagnostic imaging
Raport
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Dibutyl phthalate induced testicular dysgenesis originates after seminiferous cord formation in rats.
Autorzy:
Lara NLM; MRC Centre for Reproductive Health, The Queen's Medical Research Institute, University of Edinburgh, Edinburgh, EH16 4TJ, UK.; Laboratory of Cellular Biology, Department of Morphology, Federal University of Minas Gerais, 31270-901, Belo Horizonte/MG, Brazil.
van den Driesche S; MRC Centre for Reproductive Health, The Queen's Medical Research Institute, University of Edinburgh, Edinburgh, EH16 4TJ, UK.; Centre for Integrative Physiology, Biomedical Sciences, Hugh Robson Building, University of Edinburgh, Edinburgh, EH8 9XD, UK.
Macpherson S; MRC Centre for Reproductive Health, The Queen's Medical Research Institute, University of Edinburgh, Edinburgh, EH16 4TJ, UK.
França LR; Laboratory of Cellular Biology, Department of Morphology, Federal University of Minas Gerais, 31270-901, Belo Horizonte/MG, Brazil.; National Institute for Amazonian Research, 69067-375, Manaus/AM, Brazil.
Sharpe RM; MRC Centre for Reproductive Health, The Queen's Medical Research Institute, University of Edinburgh, Edinburgh, EH16 4TJ, UK. .
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Źródło:
Scientific reports [Sci Rep] 2017 May 31; Vol. 7 (1), pp. 2521. Date of Electronic Publication: 2017 May 31.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Dibutyl Phthalate/*toxicity
Gonadal Dysgenesis/*physiopathology
Prenatal Exposure Delayed Effects/*physiopathology
Testicular Diseases/*physiopathology
Animals ; Disease Models, Animal ; Female ; Fetus/drug effects ; Fetus/physiopathology ; Gonadal Dysgenesis/chemically induced ; Humans ; Leydig Cells/drug effects ; Leydig Cells/pathology ; Male ; Pregnancy ; Prenatal Exposure Delayed Effects/chemically induced ; Rats ; Rats, Wistar ; Seminiferous Tubules/drug effects ; Seminiferous Tubules/growth & development ; Seminiferous Tubules/pathology ; Sex Differentiation/drug effects ; Testicular Diseases/chemically induced ; Testis/drug effects ; Testis/growth & development ; Testis/pathology
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Walker-Warburg syndrome with gonadal dysgenesis: A rare association.
Autorzy:
Bera G; Department of Pathology and Neonatology, Institute of Post Graduate Medical Education & Research, Kolkata, West Bengal, India.
Halder A; Department of Pathology and Neonatology, Institute of Post Graduate Medical Education & Research, Kolkata, West Bengal, India.
Mandal B; Department of Pathology and Neonatology, Institute of Post Graduate Medical Education & Research, Kolkata, West Bengal, India.
Das RN; Department of Pathology and Neonatology, Institute of Post Graduate Medical Education & Research, Kolkata, West Bengal, India.
Mukherjee S; Department of Pathology and Neonatology, Institute of Post Graduate Medical Education & Research, Kolkata, West Bengal, India.
Chatterjee U; Department of Pathology and Neonatology, Institute of Post Graduate Medical Education & Research, Kolkata, West Bengal, India.
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Źródło:
Neurology India [Neurol India] 2017 May-Jun; Vol. 65 (3), pp. 675-677.
Typ publikacji:
Case Reports; Journal Article
MeSH Terms:
Gonadal Dysgenesis/*complications
Walker-Warburg Syndrome/*complications
Cerebellum/diagnostic imaging ; Gonadal Dysgenesis/diagnostic imaging ; Humans ; Infant ; Magnetic Resonance Imaging ; Male ; Retina/pathology ; Walker-Warburg Syndrome/diagnostic imaging
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Case report of whole genome sequencing in the XY female: identification of a novel SRY mutation and revision of a misdiagnosis of androgen insensitivity syndrome.
Autorzy:
De Sousa SM; Endocrine and Metabolic Unit, Royal Adelaide Hospital, Adelaide, SA, Australia. .; Department of Genetics and Molecular Pathology, Centre for Cancer Biology, an SA Pathology and UniSA alliance, Adelaide, SA, Australia. .; School of Medicine, University of Adelaide, Adelaide, SA, Australia. .; Hormones and Cancer Group, Garvan Institute of Medical Research, Sydney, NSW, Australia. .
Kassahn KS; Department of Genetics and Molecular Pathology, Centre for Cancer Biology, an SA Pathology and UniSA alliance, Adelaide, SA, Australia.; School of Biological Sciences, University of Adelaide, Adelaide, SA, Australia.
McIntyre LC; Department of Genetics and Molecular Pathology, Centre for Cancer Biology, an SA Pathology and UniSA alliance, Adelaide, SA, Australia.
Chong CE; Department of Genetics and Molecular Pathology, Centre for Cancer Biology, an SA Pathology and UniSA alliance, Adelaide, SA, Australia.
Scott HS; Department of Genetics and Molecular Pathology, Centre for Cancer Biology, an SA Pathology and UniSA alliance, Adelaide, SA, Australia.; School of Medicine, University of Adelaide, Adelaide, SA, Australia.; School of Biological Sciences, University of Adelaide, Adelaide, SA, Australia.; ACRF Cancer Genomics Facility, Centre for Cancer Biology, SA Pathology, Adelaide, SA, Australia.; School of Pharmacy and Medical Sciences, University of South Australia, Adelaide, SA, Australia.
Torpy DJ; Endocrine and Metabolic Unit, Royal Adelaide Hospital, Adelaide, SA, Australia.; School of Medicine, University of Adelaide, Adelaide, SA, Australia.
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Źródło:
BMC endocrine disorders [BMC Endocr Disord] 2016 Nov 08; Vol. 16 (1), pp. 58. Date of Electronic Publication: 2016 Nov 08.
Typ publikacji:
Case Reports; Journal Article
MeSH Terms:
Genome, Human*
Mutation, Missense*
Androgen-Insensitivity Syndrome/*diagnosis
Gonadal Dysgenesis, 46,XY/*diagnosis
Sex-Determining Region Y Protein/*genetics
Androgen-Insensitivity Syndrome/genetics ; DNA Mutational Analysis ; Diagnostic Errors ; Female ; Gonadal Dysgenesis, 46,XY/genetics ; Humans ; Male ; Middle Aged ; Sequence Analysis, DNA
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Cytotype Regulation Facilitates Repression of Hybrid Dysgenesis by Naturally Occurring KP Elements in Drosophila melanogaster.
Autorzy:
Simmons MJ; Department of Genetics, Cell Biology, and Development, University of Minnesota, St. Paul, Minnesota 55108-1095 .
Grimes CD; Department of Genetics, Cell Biology, and Development, University of Minnesota, St. Paul, Minnesota 55108-1095.
Czora CS; Department of Genetics, Cell Biology, and Development, University of Minnesota, St. Paul, Minnesota 55108-1095.
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Źródło:
G3 (Bethesda, Md.) [G3 (Bethesda)] 2016 Jul 07; Vol. 6 (7), pp. 1891-7. Date of Electronic Publication: 2016 Jul 07.
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:
DNA Transposable Elements*
Inheritance Patterns*
Drosophila melanogaster/*genetics
Gonadal Dysgenesis/*genetics
RNA, Small Interfering/*genetics
Animals ; Crosses, Genetic ; Drosophila melanogaster/metabolism ; Female ; Genotype ; Germ Cells/metabolism ; Gonadal Dysgenesis/metabolism ; Gonadal Dysgenesis/pathology ; HSP70 Heat-Shock Proteins/genetics ; HSP70 Heat-Shock Proteins/metabolism ; Promoter Regions, Genetic ; RNA, Small Interfering/metabolism ; Telomere/chemistry ; Telomere/metabolism ; Transgenes ; Transposases/genetics ; Transposases/metabolism
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
ЕФЕКТИ ГЕНОМНОЇ НЕСТАБІЛЬНОСТІ В ПОПУЛЯЦІЯХ DROSOPHІLA MELANOGASTER ІЗ РІЗНИХ ЗА ВПЛИВОМ РАДІАЦІЙНОГО ФАКТОРА РЕГІОНІВ УКРАЇНИ.
Autorzy:
Кравець, О. П.
Соколова, Д. О.
Ковальчук, Н. Л.
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Alternatywny tytuł:
EFFECTS OF GENOMIC INSTABILITY IN POPULATIONS OF DROSOPHILAE MELANOGASTER FROM REGIONS OF UKRAINE WITH DIFFERENT RADIATION IMPACT FACTORS.
Źródło:
Nuclear Physics & Atomic Energy. 2021, Vol. 22 Issue 2, p174-181. 8p.
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Disorders of sexual differentiation: Report of two rare cases.
Autorzy:
Correya MA; Department of Pathology, Sri Ramachandra Institute of Higher Education and Research, Chennai, Tamil Nadu, India.
Babu R; Department of Paediatric Urology, Sri Ramachandra Institute of Higher Education and Research, Chennai, Tamil Nadu, India.
Archana B; Department of Pathology, Sri Ramachandra Institute of Higher Education and Research, Chennai, Tamil Nadu, India.
Ravirajendiran S; Department of Paediatric Urology, Sri Ramachandra Institute of Higher Education and Research, Chennai, Tamil Nadu, India.
Pokaż więcej
Źródło:
Indian journal of pathology & microbiology [Indian J Pathol Microbiol] 2021 Apr-Jun; Vol. 64 (2), pp. 390-393.
Typ publikacji:
Case Reports; Journal Article
MeSH Terms:
Sex Chromosome Aberrations*
Disorders of Sex Development/*physiopathology
Gonadal Dysgenesis, Mixed/*physiopathology
Sex Differentiation/*physiology
Abnormal Karyotype ; Adolescent ; Chromosome Deletion ; Cryptorchidism/genetics ; Female ; Humans ; Hypospadias/physiopathology ; Infant ; Male ; Mosaicism ; Primitive Streak/embryology ; Testis/abnormalities ; Uterus/abnormalities
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Extragonadal recurrence of benign mature teratoma in the pouch of Douglas.
Autorzy:
Sato, Miho
Nasu, Kaei
Matsumoto, Harunobu
Konishi, Kota
Yasumi, Shunsuke
Sato, Yusuke
Yano, Mitsutake
Kobayashi, Eiji
Pokaż więcej
Temat:
TERATOMA
TRANSVAGINAL ultrasonography
RESTORATIVE proctocolectomy
GONADAL dysgenesis
MAGNETIC resonance imaging
BENIGN tumors
JAPANESE women
ANTI-NMDA receptor encephalitis
Źródło:
Asian Journal of Endoscopic Surgery; Jan2024, Vol. 17 Issue 1, p1-4, 4p
Czasopismo naukowe
Szczegóły
Tytuł:
Behavioral Assessment of Central Auditory Processing in Turner Syndrome.
Autorzy:
Santos, Adriana Fernandes Duarte dos
Bazilio, Martha Marcela Matos
Frota, Silvana
Guimarães, Marilia
Ribeiro, Marcia Gonçalves
Pokaż więcej
Temat:
AUDITORY perception
TURNER'S syndrome
BEHAVIORAL assessment
SEX chromosomes
X chromosome
WORD deafness
GONADAL dysgenesis
Źródło:
International Archives of Otorhinolaryngology; Jan2024, Vol. 28 Issue 1, pe50-e56, 7p
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Wyświetlanie 61-80 z 2626

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