Supernumerary marker 15 chromosome in a patient with Prader-Willi syndrome [1]

Clinical Genetics

Volumn 65, Issue 3, 2004, Pages 242-243

  Borelina, D ^b   Esperante, S ^b   Gutnisky, V ^b   Ferreiro, V ^b   Ferrer, M ^b   Giliberto, F ^b   Frechtel, G ^b   Francipane, L ^b   Szijan, Irene ^a  

^a UNIVERSIDAD DE BUENOS AIRES   (Argentina)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ALLELE; CASE REPORT; CENTROMERE; CHROMOSOME 15; CHROMOSOME ANALYSIS; CHROMOSOME ARM; CHROMOSOME DELETION; CHROMOSOME REARRANGEMENT; DISOMY; DIZYGOTIC TWINS; DNA METHYLATION; DNA POLYMORPHISM; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENETIC MARKER; HETEROZYGOSITY; HUMAN; HYPERPHAGIA; HYPOGONADISM; HYPOPIGMENTATION; INSULIN DEPENDENT DIABETES MELLITUS; KARYOTYPE; LETTER; MARKER CHROMOSOME; MEIOSIS; MENTAL DEFICIENCY; MUSCLE HYPOTONIA; OBESITY; PHENOTYPE; PRADER WILLI SYNDROME; PRIORITY JOURNAL; SUPERNUMERARY CHROMOSOME;

ADOLESCENT; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 15; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INHERITANCE PATTERNS; PRADER-WILLI SYNDROME; UNIPARENTAL DISOMY;

EID: 1242263316     PISSN: 00099163     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.0009-9163.2004.00203.x     Document Type: Letter

References (9)

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