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Wyszukujesz frazę ""Chromosomes, Human, Pair 17 genetics"" wg kryterium: Temat


Wyświetlanie 1-11 z 11
Tytuł :
Congenital Generalized Hypertrichosis Terminalis with Gingival Hyperplasia and a Coarse Face: a Case Report
Autorzy :
Kazandjieva Jana
Stefanova Elisaveta
Todorova Zdravka
Nikolova Gergovska Malena
Semkova Kristina
Pokaż więcej
Temat :
Hypertrichosis + congenital
Gingival Hyperplasia
Chromosomes, Human, Pair 17 + genetics
Child
Hydronephrosis
Case Reports
Dermatology
RL1-803
Źródło :
Serbian Journal of Dermatology and Venereology, Vol 8, Iss 1, Pp 5-12 (2016)
Opis pliku :
electronic resource
Relacje :
http://www.degruyter.com/view/j/sjdv.2016.8.issue-1/sjdv-2016-0001/sjdv-2016-0001.xml?format=INT; https://doaj.org/toc/1821-0902; https://doaj.org/toc/2406-0631
Dostęp URL :
https://doaj.org/article/6052583dcb374971be8cf608e2ef1045
Czasopismo naukowe
Tytuł :
Correction for chromosome-17 is critical for the determination of true Her-2/neu gene amplification status in breast cancer
Index Terms :
Sciences bio-médicales et agricoles
Aneuploidy
Breast Neoplasms -- genetics
Breast Neoplasms -- metabolism
Chromosomes, Human, Pair 17 -- genetics
Female
Humans
In Situ Hybridization, Fluorescence
Nucleic Acid Amplification Techniques
RNA, Messenger -- biosynthesis
Receptor, erbB-2 -- biosynthesis
Receptor, erbB-2 -- genetics
info:eu-repo/semantics/article
info:ulb-repo/semantics/articlePeerReview
info:ulb-repo/semantics/openurl/article
URL :
http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/54753">http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/54753
http://worldcat.org/search?q=on:EQY+http://difusion-oai.ulb.ac.be/oai/request+DCG_ENTIRE_REPOSITORY+CNTCOLL">http://worldcat.org/search?q=on:EQY+http://difusion-oai.ulb.ac.be/oai/request+DCG_ENTIRE_REPOSITORY+CNTCOLL
Zasób elektroniczny
Tytuł :
Congenital stationary night blindness: report of an autosomal recessive family and linkage analysis.
Index Terms :
Sciences bio-médicales et agricoles
Child, Preschool
Chromosomes, Human, Pair 17 -- genetics
Chromosomes, Human, Pair 7 -- genetics
Chromosomes, Human, X -- genetics
Consanguinity
DNA Mutational Analysis
Family Health
Female
Fragile X Mental Retardation Protein
Genes, Recessive -- genetics
Haplotypes
Humans
Linkage (Genetics)
Male
Microsatellite Repeats
Nerve Tissue Proteins -- genetics
Night Blindness -- congenital
Night Blindness -- genetics
Pedigree
RNA-Binding Proteins -- genetics
Receptors, Androgen -- genetics
Trinucleotide Repeats -- genetics
Hemeralopia
Homozygosity mapping
Nyctalopia
ON pathway
Synaptic connectivity
info:eu-repo/semantics/article
info:ulb-repo/semantics/articlePeerReview
info:ulb-repo/semantics/openurl/article
URL :
http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/53594">http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/53594
http://worldcat.org/search?q=on:EQY+http://difusion-oai.ulb.ac.be/oai/request+DCG_ENTIRE_REPOSITORY+CNTCOLL">http://worldcat.org/search?q=on:EQY+http://difusion-oai.ulb.ac.be/oai/request+DCG_ENTIRE_REPOSITORY+CNTCOLL
Zasób elektroniczny
Tytuł :
Polysomy 17 in HER-2/neu status elaboration in breast cancer: effect on daily practice
Index Terms :
Cancérologie
Médecine pathologie humaine
Sciences bio-médicales et agricoles
Breast Neoplasms -- genetics
Breast Neoplasms -- metabolism
Breast Neoplasms -- pathology
Chromosome Aberrations
Chromosomes, Human, Pair 17 -- genetics
Female
Gene Dosage
Humans
Immunohistochemistry
In Situ Hybridization, Fluorescence
Receptor, erbB-2 -- analysis
Receptor, erbB-2 -- genetics
info:eu-repo/semantics/article
info:ulb-repo/semantics/articlePeerReview
info:ulb-repo/semantics/openurl/article
URL :
http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/54538">http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/54538
http://worldcat.org/search?q=on:EQY+http://difusion-oai.ulb.ac.be/oai/request+DCG_ENTIRE_REPOSITORY+CNTCOLL">http://worldcat.org/search?q=on:EQY+http://difusion-oai.ulb.ac.be/oai/request+DCG_ENTIRE_REPOSITORY+CNTCOLL
Zasób elektroniczny
Tytuł :
Familial frontotemporal dementia with ubiquitin-positive inclusions is linked to chromosome 17q21-22
Index Terms :
Linkage (Genetics)
Aged
Chromosomes, Human, Pair 17/*genetics
Dementia/*genetics/pathology/psychology
Female
Humans
Inclusion Bodies/genetics/metabolism/*pathology
Male
Middle aged
Pedigree
Research Support, Non-U.S. Gov't
Ubiquitins/*analysis/genetics
tau Proteins/analysis/genetics
info:eu-repo/semantics/article
Źródło :
Brain: a journal of neurology
URL :
http://repub.eur.nl/pub/9764">http://repub.eur.nl/pub/9764
Zasób elektroniczny
Tytuł :
Physical mapping of the CC-chemokine gene cluster on the human 17q11. 2 region.
Index Terms :
Sciences bio-médicales et agricoles
Chemokines, CC -- genetics
Chromosomes, Bacterial
Chromosomes, Human, Pair 17 -- genetics
Contig Mapping
DNA -- genetics
DNA -- metabolism
Humans
Hybrid Cells
In Situ Hybridization, Fluorescence
Multigene Family -- genetics
Physical Chromosome Mapping
info:eu-repo/semantics/article
info:ulb-repo/semantics/articlePeerReview
info:ulb-repo/semantics/openurl/article
URL :
http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/57875">http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/57875
http://worldcat.org/search?q=on:EQY+http://difusion-oai.ulb.ac.be/oai/request+DCG_ENTIRE_REPOSITORY+CNTCOLL">http://worldcat.org/search?q=on:EQY+http://difusion-oai.ulb.ac.be/oai/request+DCG_ENTIRE_REPOSITORY+CNTCOLL
Zasób elektroniczny
Tytuł :
Alveolar soft-part sarcoma: further evidence by FISH for the involvement of chromosome band 17q25.
Index Terms :
Sciences bio-médicales et agricoles
Child
Chromosome Banding
Chromosomes, Human, Pair 17 -- genetics
Chromosomes, Human, Pair 17 -- ultrastructure
Female
Humans
In Situ Hybridization, Fluorescence
Sarcoma, Alveolar Soft Part -- genetics
Sarcoma, Alveolar Soft Part -- ultrastructure
Uterine Neoplasms -- genetics
Uterine Neoplasms -- ultrastructure
info:eu-repo/semantics/article
info:ulb-repo/semantics/articlePeerReview
info:ulb-repo/semantics/openurl/article
URL :
http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/57915">http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/57915
http://worldcat.org/search?q=on:EQY+http://difusion-oai.ulb.ac.be/oai/request+DCG_ENTIRE_REPOSITORY+CNTCOLL">http://worldcat.org/search?q=on:EQY+http://difusion-oai.ulb.ac.be/oai/request+DCG_ENTIRE_REPOSITORY+CNTCOLL
Zasób elektroniczny
Tytuł :
Haploinsufficiency of cytosolic serine hydroxymethyltransferase in the Smith-Magenis syndrome.
Index Terms :
Sciences bio-médicales et agricoles
Abnormalities, Multiple -- genetics
Base Sequence
Chromosome Mapping
Chromosomes, Human, Pair 17 -- genetics
Gene Deletion
Glycine Hydroxymethyltransferase -- blood
Glycine Hydroxymethyltransferase -- genetics
Glycine Hydroxymethyltransferase -- urine
Humans
Mental Retardation -- genetics
Molecular Sequence Data
info:eu-repo/semantics/article
info:ulb-repo/semantics/articlePeerReview
info:ulb-repo/semantics/openurl/article
URL :
http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/58603">http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/58603
http://worldcat.org/search?q=on:EQY+http://difusion-oai.ulb.ac.be/oai/request+DCG_ENTIRE_REPOSITORY+CNTCOLL">http://worldcat.org/search?q=on:EQY+http://difusion-oai.ulb.ac.be/oai/request+DCG_ENTIRE_REPOSITORY+CNTCOLL
Zasób elektroniczny
    Wyświetlanie 1-11 z 11

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