Analysis of parent of origin specific DNA methylation at SNRPN and PW71 in tissues: Implication for prenatal diagnosis

Journal of Medical Genetics

Volumn 33, Issue 12, 1996, Pages 1011-1014

  Kubota, Takeo ^a   Aradhya, Swaroop ^b   Macha, Michelle ^b   Smith, Ann C M ^b   Surh, Linda C ^c   Satish, Jayavanthi ^d   Verp, Marion S ^e   Nee, Holly L ^f   Johnson, Anthony ^f   Christian, Susan L ^a   Ledbetter, David H ^a,e  

^a NATIONAL HUMAN GENOME RESEARCH INSTITUTE   (United States)

^b GEORGETOWN UNIVERSITY MEDICAL CENTER   (United States)

^c CHILDREN S HOSPITAL OF EASTERN ONTARIO   (Canada)

^d SINAI HOSPITAL OF BALTIMORE   (United States)

^e UNIVERSITY OF CHICAGO   (United States)

^f Prenatal Diagnostic Center   (United States)

Author keywords

Prader Willi Angelman syndromes; Prenatal diagnosis; PW71 methylation; SNRPN methylation

Indexed keywords

POLYPEPTIDE; SMALL NUCLEAR RIBONUCLEOPROTEIN;

AMNIOTIC FLUID CELL; ARTICLE; CHORION VILLUS; CHROMOSOME 15Q; DEVELOPMENTAL DISORDER; DNA METHYLATION; DNA POLYMORPHISM; FETUS; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DELETION; HAPPY PUPPET SYNDROME; HUMAN; HUMAN CELL; HUMAN TISSUE; LYMPHOBLAST; PRADER WILLI SYNDROME; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; SOUTHERN BLOTTING;

EID: 16944366031     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: 10.1136/jmg.33.12.1011     Document Type: Article

References (16)

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