Angelman and Prader-Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion.

American journal of medical genetics

Volumn 32, Issue 2, 1989, Pages 285-290

  Knoll, J H ^a   Nicholls, R D ^a   Magenis, R E ^a   Graham Jr , J M ^a   Lalande, M ^a   Latt, S A ^a  

^a BOSTON CHILDREN S HOSPITAL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA;

ARTICLE; CHILD; CHROMOSOME 15; CHROMOSOME DELETION; EPILEPSY; GENETICS; HUMAN; MENTAL DEFICIENCY; MICROCEPHALY; PRADER WILLI SYNDROME; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; SYNDROME;

CHILD; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 15; DNA; EPILEPSY; HUMANS; MENTAL RETARDATION; MICROCEPHALY; POLYMORPHISM, RESTRICTION FRAGMENT LENGTH; PRADER-WILLI SYNDROME; SYNDROME;

EID: 0024619007     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.1320320235     Document Type: Article

References (0)