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Molecular breakpoint cloning and gene expression studies of a novel translocation t(4;15)(q27;q11.2) associated with Prader-Willi syndromeSnoRNA Snord116 (Pwcr1/MBII-85) deletion causes growth deficiency and hyperphagia in micePrader-Willi syndromeSmall evolutionarily conserved RNA, resembling C/D box small nucleolar RNA, is transcribed from PWCR1, a novel imprinted gene in the Prader-Willi deletion region, which Is highly expressed in brainIdentification of novel imprinted transcripts in the Prader-Willi syndrome and Angelman syndrome deletion region: further evidence for regional imprinting controlPrader-Willi syndrome is caused by disruption of the SNRPN geneEffect of growth hormone on height, weight, and body composition in Prader-Willi syndromeGene structure, DNA methylation, and imprinted expression of the human SNRPN genePrevalence of overweight in children and adolescents with attention deficit hyperactivity disorder and autism spectrum disorders: a chart reviewImprinting disorders: a group of congenital disorders with overlapping patterns of molecular changes affecting imprinted lociGenetics of Prader-Willi syndrome and Prader-Will-Like syndromeDecreased bone mineral density in Prader-Willi syndrome: comparison with obese subjectsReward processing in autism: a thematic series.Sleep, plasticity and the pathophysiology of neurodevelopmental disorders: the potential roles of protein synthesis and other cellular processes.Severe tooth wear in Prader-Willi syndrome. A case-control study.Postural adaptations to long-term training in Prader-Willi patients.Strength characterization of knee flexor and extensor muscles in Prader-Willi and obese patients.Neonatal maternal deprivation response and developmental changes in gene expression revealed by hypothalamic gene expression profiling in mice.Genomic imprinting: implications for human disease.Practice guidelines for the molecular analysis of Prader-Willi and Angelman syndromes.The Prader-Willi syndrome.Diagnosis in Prader-Willi syndrome.DNA methylation based testing of 450 patients suspected of having Prader-Willi syndromeFamilial translocations involving 15q11-q13 can give rise to interstitial deletions causing Prader-Willi or Angelman syndrome.Prader-Willi syndrome in a child with mosaic trisomy 15 and mosaic triplo-X: a molecular analysis.Trisomy 15 rescue with jumping translocation of distal 15q in Prader-Willi syndrome.Counselling dilemmas associated with the molecular characterisation of two Angelman syndrome families.Molecular screening for proximal 15q abnormalities in a mentally retarded population.Nutritient intake of young children with Prader-Willi syndrome.Respiratory Depression in Young Prader Willi Syndrome Patients following Clonidine Provocation for Growth Hormone Secretion Testing.Behavioral Health in Developmental Disabilities: A Comprehensive Program of Nutrition, Exercise, and Weight Reduction.Severe Short Stature in an Adolescent Male with Prader-Willi Syndrome and Congenital Adrenal Hyperplasia: A Therapeutic ConundrumClinical management of behavioral characteristics of Prader-Willi syndrome.Treatment of scoliosis in patients affected with Prader-Willi syndrome using various techniquesGait patterns in Prader-Willi and Down syndrome patients.A paternal deletion of MKRN3, MAGEL2 and NDN does not result in Prader-Willi syndromeDifferent distribution of the genetic subtypes of the Prader-Willi syndrome in the elderly.The E6-Ap ubiquitin-protein ligase (UBE3A) gene is localized within a narrowed Angelman syndrome critical region.Psychiatric adverse effects of rimonobant in adults with Prader Willi syndromePET scan perfusion imaging in the Prader-Willi syndrome: new insights into the psychiatric and social disturbances.
P2860
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P2860
description
1993 nî lūn-bûn
@nan
1993 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
1993 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
1993年の論文
@ja
1993年論文
@yue
1993年論文
@zh-hant
1993年論文
@zh-hk
1993年論文
@zh-mo
1993年論文
@zh-tw
1993年论文
@wuu
name
Prader-Willi syndrome: consensus diagnostic criteria.
@ast
Prader-Willi syndrome: consensus diagnostic criteria.
@en
Prader-Willi syndrome: consensus diagnostic criteria.
@nl
type
label
Prader-Willi syndrome: consensus diagnostic criteria.
@ast
Prader-Willi syndrome: consensus diagnostic criteria.
@en
Prader-Willi syndrome: consensus diagnostic criteria.
@nl
prefLabel
Prader-Willi syndrome: consensus diagnostic criteria.
@ast
Prader-Willi syndrome: consensus diagnostic criteria.
@en
Prader-Willi syndrome: consensus diagnostic criteria.
@nl
P2093
P1433
P1476
Prader-Willi syndrome: consensus diagnostic criteria
@en
P2093
B Y Whitman
F Greenberg
J M Hanchett
L R Greenswag
M G Butler
S B Cassidy
P304
P407
P577
1993-02-01T00:00:00Z