Prader Willi syndrome patients: Study of 77 patients;Síndrome de Prader Willi: Estudio de 77 pacientes

Medicina Clinica

Volumn 133, Issue 17, 2009, Pages 649-656

  Poyatos, David ^a   Camprubí, Cristina ^a   Gabau, Elisabeth ^b   Nosas, Ramón ^b   Villatoro, Sergi ^b   Coll, María Dolores ^a   Guitart, Miriam ^b  

^a UNIVERSITAT AUTÒNOMA DE BARCELONA   (Spain)

^b HOSPITAL DE SABADELL   (Spain)

Author keywords

Genetic disease; Prader Willi syndrome; Uniparental disomy

Indexed keywords

ARTICLE; CHILD; CLINICAL FEATURE; CYTOGENETICS; FEMALE; FISH; GASTRIC BANDING; GENE DELETION; GENETIC ANALYSIS; GENOTYPE PHENOTYPE CORRELATION; HUMAN; MAJOR CLINICAL STUDY; MALE; MASS SPECTROMETRY; METHYLATION; MICROSATELLITE INSTABILITY; MOLECULAR GENETICS; POLYMERASE CHAIN REACTION; PRADER WILLI SYNDROME; PRESCHOOL CHILD; SCHOOL CHILD; SOUTHERN BLOTTING; UNIPARENTAL DISOMY;

ADOLESCENT; ADULT; ALGORITHMS; CHILD; CHILD, PRESCHOOL; CROSS-SECTIONAL STUDIES; FEMALE; HUMANS; INFANT; MALE; PRADER-WILLI SYNDROME; YOUNG ADULT;

EID: 70350565507     PISSN: 00257753     EISSN: 15788989     Source Type: Journal    
DOI: 10.1016/j.medcli.2009.04.051     Document Type: Article

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