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Genetic Testing

Volumn 4, Issue 4, 2000, Pages 387-392

Prader-Willi syndrome: Genetic tests and clinical findings

(5) Fridman, C a Varela, M C a Kok, F a Setian, N a Koiffmann, C P a

a UNIVERSITY OF SÃO PAULO (Brazil)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; BODY HEIGHT; CHILD; CLINICAL FEATURE; CONTROLLED STUDY; EARLY DIAGNOSIS; FEMALE; GENE DELETION; GENE LOCUS; GENE MAPPING; GENETIC ANALYSIS; HUMAN; HUMAN CELL; MAJOR CLINICAL STUDY; MALE; METHYLATION; PHENOTYPE; PRADER WILLI SYNDROME; UNIPARENTAL DISOMY;

ADOLESCENT; ADULT; CHILD; CHILD, PRESCHOOL; COHORT STUDIES; DNA METHYLATION; FEMALE; GENOTYPE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; LYMPHOCYTES; MALE; MICROSATELLITE REPEATS; PHENOTYPE; PRADER-WILLI SYNDROME; SEQUENCE DELETION;

EID: 0034509987 PISSN: 10906576 EISSN: None Source Type: Journal
DOI: 10.1089/109065700750065144 Document Type: Article

Times cited : (23)

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