Genotype-phenotype correlation in a series of 167 deletion and non-deletion patients with Prader-Willi syndrome.
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Prader-Willi syndromeGenetics of Prader-Willi syndrome and Prader-Will-Like syndromePrader-Willi and Angelman syndromes: sister imprinted disordersImprinted segments in the human genome: different DNA methylation patterns in the Prader-Willi/Angelman syndrome region as determined by the genomic sequencing methodPsychosis and autism as diametrical disorders of the social brainFrench database of children and adolescents with Prader-Willi syndrome.Prader-Willi syndrome in a child with mosaic trisomy 15 and mosaic triplo-X: a molecular analysis.A long-term population-based clinical and morbidity review of Prader-Willi syndrome in Western Australia.Prader-Willi syndrome: an update and review for the primary pediatrician.Genetic subtype differences in neural circuitry of food motivation in Prader-Willi syndrome.Prader-Willi Syndrome: Clinical and Genetic FindingsDoes the Genetic Cause of Prader-Willi Syndrome Explain the Highly Variable Phenotype?Prader-Willi Syndrome: A spectrum of anatomical and clinical features.Growth patterns of Chinese patients with Prader-Willi syndrome.Prader-willi syndrome: clinical aspectsNutrient intake and body composition variables in Prader-Willi syndrome--effect of growth hormone supplementation and genetic subtype.Cross-cultural comparisons of obesity and growth in Prader-Willi syndrome.Prader-Willi syndrome: intellectual abilities and behavioural features by genetic subtype.Prader-Willi syndrome: new insights in the behavioural and psychiatric spectrum.Comparison of phenotype in uniparental disomy and deletion Prader-Willi syndrome: sex specific differences.Prader-Willi syndrome.Maladaptive behaviors and risk factors among the genetic subtypes of Prader-Willi syndrome.Prader-Willi syndrome.Phenotypic heterogeneity of growth and psychometric intelligence in Prader-Willi syndrome: variable expression of a contiguous gene syndrome or parent-child resemblance?Intellectual characteristics of Prader-Willi syndrome: comparison of genetic subtypes.Clinical and genetic features of Prader-Willi syndrome in China.Mosaic imprinting defect in a patient with an almost typical expression of the Prader-Willi syndrome.Microdeletion Syndromes
P2860
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P2860
Genotype-phenotype correlation in a series of 167 deletion and non-deletion patients with Prader-Willi syndrome.
description
1995 nî lūn-bûn
@nan
1995年の論文
@ja
1995年学术文章
@wuu
1995年学术文章
@zh-cn
1995年学术文章
@zh-hans
1995年学术文章
@zh-my
1995年学术文章
@zh-sg
1995年學術文章
@yue
1995年學術文章
@zh
1995年學術文章
@zh-hant
name
Genotype-phenotype correlation ...... ts with Prader-Willi syndrome.
@en
Genotype-phenotype correlation ...... ts with Prader-Willi syndrome.
@nl
type
label
Genotype-phenotype correlation ...... ts with Prader-Willi syndrome.
@en
Genotype-phenotype correlation ...... ts with Prader-Willi syndrome.
@nl
prefLabel
Genotype-phenotype correlation ...... ts with Prader-Willi syndrome.
@en
Genotype-phenotype correlation ...... ts with Prader-Willi syndrome.
@nl
P2093
P356
P1433
P1476
Genotype-phenotype correlation ...... ts with Prader-Willi syndrome.
@en
P2093
B Horsthemke
E Passarge
G Gillessen-Kaesbach
S Kaya-Westerloh
W Robinson
P2888
P304
P356
10.1007/BF00210291
P577
1995-12-01T00:00:00Z