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-q12Synchrony of oculocutaneous albinism, the Prader-Willi syndrome, and a normal karyotypePrader-Willi syndrome: current understanding of cause and diagnosis.Hypopigmentation: a common feature of Prader-Labhart-Willi syndrome.Molecular, cytogenetic, and clinical investigations of Prader-Willi syndrome patients.The tyrosinase-positive oculocutaneous albinism gene shows locus homogeneity on chromosome 15q11-q13 and evidence of multiple mutations in southern African negroids.AMINO ACID LEVELS IN PRADER-WILLI SYNDROME AND OBESE INDIVIDUALS.
P2860
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P2860
description
1987 nî lūn-bûn
@nan
1987 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
1987 թվականի մայիսին հրատարակված գիտական հոդված
@hy
1987年の論文
@ja
1987年論文
@yue
1987年論文
@zh-hant
1987年論文
@zh-hk
1987年論文
@zh-mo
1987年論文
@zh-tw
1987年论文
@wuu
name
Hypopigmentation in the Prader-Willi syndrome
@ast
Hypopigmentation in the Prader-Willi syndrome
@en
type
label
Hypopigmentation in the Prader-Willi syndrome
@ast
Hypopigmentation in the Prader-Willi syndrome
@en
prefLabel
Hypopigmentation in the Prader-Willi syndrome
@ast
Hypopigmentation in the Prader-Willi syndrome
@en
P2093
P2860
P1476
Hypopigmentation in the Prader-Willi syndrome
@en
P2093
P2860
P304
P407
P577
1987-05-01T00:00:00Z