Prader-Willi syndrome due to 15q11-q13 deletion in a girl with an inherited (13;14) Robertsonian translocation [1]

American Journal of Medical Genetics

Volumn 113, Issue 3, 2002, Pages 307-308

  Alliende, Angélica ^a   Curotto, Bianca ^a   Maria, Lorena Santa ^a   Cortés, Fanny ^a   Aracena, Mariana ^b  

^a UNIVERSITY OF CHILE   (Chile)

^b HOSPITAL LUIS CALVO MACKENNA   (Chile)

Author keywords

[No Author keywords available]

Indexed keywords

CASE REPORT; CHROMOSOME 15Q; CHROMOSOME DELETION; CHROMOSOME REARRANGEMENT; CHROMOSOME TRANSLOCATION 13; CHROMOSOME TRANSLOCATION 14; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; LETTER; PRADER WILLI SYNDROME; PRESCHOOL CHILD; PRIORITY JOURNAL; ROBERTSONIAN CHROMOSOME TRANSLOCATION; CHROMOSOME 15; DNA METHYLATION; GENE DELETION; GENE TRANSLOCATION; GENETICS; INFANT; NEWBORN;

ROBERTSONIA;

CHILD, PRESCHOOL; CHROMOSOMES, HUMAN, PAIR 15; DNA METHYLATION; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; INFANT, NEWBORN; PRADER-WILLI SYNDROME; SEQUENCE DELETION; TRANSLOCATION, GENETIC;

EID: 0036889099     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.10799     Document Type: Letter

References (13)

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