Temat: "Chromosomes, Human, Pair 13" - OpacWWW

Skocz do pozycji: 1.

Tytuł:: Misgivings.
Autorzy:: Farlow B; Canadian Patient Safety Institute.; Pokaż więcej
Źródło:: The Hastings Center report [Hastings Cent Rep] 2009 Sep-Oct; Vol. 39 (5), pp. 19-21.
Typ publikacji:: Case Reports; Journal Article
MeSH Terms:: Chromosomes, Human, Pair 13*
Parents*/psychology
Patient Advocacy*
Respiratory Insufficiency*/etiology
Social Values*
Withholding Treatment*
Abnormalities, Multiple/*genetics
Trisomy/*diagnosis
Adult ; Diagnostic Errors ; Fatal Outcome ; Female ; Health Care Rationing ; Humans ; Infant, Newborn ; Narration ; Pneumonia/complications ; Pneumonia/diagnosis ; Prenatal Diagnosis ; Trust

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Skocz do pozycji: 2.

Tytuł:: Genome sequencing identifies a large deletion at 13q32.1 as the cause of microcoria and childhood-onset glaucoma.
Autorzy:: Sergouniotis PI; Manchester Royal Eye Hospital, Central Manchester University Hospitals NHS Foundation Trust, Manchester Academic Health Science Centre, Manchester, UK.; Centre for Genomic Medicine, Central Manchester University Hospitals NHS Foundation Trust, Manchester Academic Health Science Centre, Manchester, UK.; Centre for Ophthalmology & Vision Sciences, Institute of Human Development, Faculty of Medical and Human Sciences, University of Manchester, Manchester, UK.
Ellingford JM; Centre for Genomic Medicine, Central Manchester University Hospitals NHS Foundation Trust, Manchester Academic Health Science Centre, Manchester, UK.
O'Sullivan J; Centre for Genomic Medicine, Central Manchester University Hospitals NHS Foundation Trust, Manchester Academic Health Science Centre, Manchester, UK.
Fenerty CH; Manchester Royal Eye Hospital, Central Manchester University Hospitals NHS Foundation Trust, Manchester Academic Health Science Centre, Manchester, UK.; Centre for Ophthalmology & Vision Sciences, Institute of Human Development, Faculty of Medical and Human Sciences, University of Manchester, Manchester, UK.
Black GC; Centre for Genomic Medicine, Central Manchester University Hospitals NHS Foundation Trust, Manchester Academic Health Science Centre, Manchester, UK.; Centre for Ophthalmology & Vision Sciences, Institute of Human Development, Faculty of Medical and Human Sciences, University of Manchester, Manchester, UK.; Pokaż więcej
Źródło:: Acta ophthalmologica [Acta Ophthalmol] 2017 May; Vol. 95 (3), pp. e249-e250. Date of Electronic Publication: 2016 Sep 28.
Typ publikacji:: Letter
MeSH Terms:: Point Mutation*
Chromosomes, Human, Pair 13/*genetics
Eye Proteins/*genetics
Genetic Testing/*methods
Glaucoma/*genetics
Pupil Disorders/*congenital
Adolescent ; Adult ; Child ; Eye Proteins/metabolism ; Female ; Genotype ; Glaucoma/diagnosis ; Glaucoma/metabolism ; Humans ; Male ; Pedigree ; Pupil Disorders/diagnosis ; Pupil Disorders/genetics ; Pupil Disorders/metabolism ; Young Adult
SCR Disease Name:: Microcoria, congenital

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Tytuł:: Mapping of the oncogene c-myc (MYC) and the breast cancer susceptibility gene (BRCA2) in the pig by FISH.
Autorzy:: Musilová P; Veterinary Research Institute, Brno, Czech Republic. />Kubícková S
Vozdová M
Rubes J; Pokaż więcej
Źródło:: Animal genetics [Anim Genet] 2000 Apr; Vol. 31 (2), pp. 154.
Typ publikacji:: Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:: Chromosome Mapping/*veterinary
Genes, myc/*genetics
In Situ Hybridization, Fluorescence/*veterinary
Neoplasm Proteins/*genetics
Swine/*genetics
Transcription Factors/*genetics
Animals ; BRCA2 Protein ; Chromosomes, Human, Pair 13 ; Genetic Linkage ; Humans

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Tytuł:: Physical assignments of human chromosome 13 genes on pig chromosome 11 demonstrate extensive synteny and gene order conservation between pig and human.
Autorzy:: Sun HS; Department of Animal Science, Iowa State University, USA.
Yerle M
Pinton P
Chardon P
Rogel-Gaillard C
Lyons LA
Laughlin TF
Tuggle CK; Pokaż więcej
Źródło:: Animal genetics [Anim Genet] 1999 Aug; Vol. 30 (4), pp. 304-8.
Typ publikacji:: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.
MeSH Terms:: Physical Chromosome Mapping*
Swine/*genetics
Animals ; Biological Evolution ; Cattle ; Chromosomes, Human, Pair 13/genetics ; Gene Rearrangement ; Humans ; In Situ Hybridization, Fluorescence ; Species Specificity

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