Hypopigmentation: a common feature of Prader-Labhart-Willi syndrome.
about
Prader-Willi syndromeThree genome-wide association studies and a linkage analysis identify HERC2 as a human iris color geneThe tyrosinase-positive oculocutaneous albinism locus maps to chromosome 15q11.2-q12Expression of 4 genes between chromosome 15 breakpoints 1 and 2 and behavioral outcomes in Prader-Willi syndromePrader-Willi syndrome: current understanding of cause and diagnosis.Prader-Willi Syndrome: Obesity due to Genomic Imprinting.Coding and noncoding expression patterns associated with rare obesity-related disorders: Prader-Willi and Alström syndromes.Evaluation of potential models for imprinted and nonimprinted components of human chromosome 15q11-q13 syndromes by fine-structure homology mapping in the mouse.Prader-Willi syndrome: a review of clinical, genetic, and endocrine findings.Prader-Willi Syndrome: Clinical and Genetic FindingsEVALUATION OF PLASMA SUBSTANCE P AND BETA-ENDORPHIN LEVELS IN CHILDREN WITH PRADER-WILLI SYNDROME.Prader-Willi Syndrome: Genetics and BehaviorBenefits and limitations of prenatal screening for Prader-Willi syndrome.Growth Charts for Prader-Willi Syndrome During Growth Hormone Treatment.Prader-willi syndrome: clinical aspectsAMINO ACID LEVELS IN PRADER-WILLI SYNDROME AND OBESE INDIVIDUALS.Prader-Willi syndrome.A 5-year-old white girl with Prader-Willi syndrome and a submicroscopic deletion of chromosome 15q11q13.
P2860
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P2860
Hypopigmentation: a common feature of Prader-Labhart-Willi syndrome.
description
1989 nî lūn-bûn
@nan
1989 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
1989 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
1989年の論文
@ja
1989年論文
@yue
1989年論文
@zh-hant
1989年論文
@zh-hk
1989年論文
@zh-mo
1989年論文
@zh-tw
1989年论文
@wuu
name
Hypopigmentation: a common feature of Prader-Labhart-Willi syndrome.
@ast
Hypopigmentation: a common feature of Prader-Labhart-Willi syndrome.
@en
type
label
Hypopigmentation: a common feature of Prader-Labhart-Willi syndrome.
@ast
Hypopigmentation: a common feature of Prader-Labhart-Willi syndrome.
@en
prefLabel
Hypopigmentation: a common feature of Prader-Labhart-Willi syndrome.
@ast
Hypopigmentation: a common feature of Prader-Labhart-Willi syndrome.
@en
P2860
P1476
Hypopigmentation: a common feature of Prader-Labhart-Willi syndrome
@en
P2093
M G Butler
P2860
P304
P407
P577
1989-07-01T00:00:00Z