Prospective prenatal diagnosis of Prader-Willi syndrome due to maternal disomy for chromosome 15 following trisomic zygote rescue

Prenatal Diagnosis

Volumn 17, Issue 8, 1997, Pages 780-783

  Roberts, Eileen ^a,c   Stevenson, K ^a   Cole, T ^a   Redford, D H A ^b   Davison, E V ^a  

^a BIRMINGHAM WOMEN S HOSPITAL   (United Kingdom)

^b PRINCESS ROYAL HOSPITAL   (United Kingdom)

^c BIRMINGHAM CHILDREN S HOSPITAL NHS FOUNDATION TRUST   (United Kingdom)

Author keywords

Maternal disomy; Trisomy 15 CVS

Indexed keywords

ADULT; ALLELE; AMNIOCENTESIS; AMNION CELL; ARTICLE; CASE REPORT; CHORION VILLUS SAMPLING; CHROMOSOME 15; FEMALE; GENE LOCUS; HUMAN; KARYOTYPE; MOLECULAR GENETICS; PRADER WILLI SYNDROME; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; UNIPARENTAL DISOMY;

ADULT; AMNIOCENTESIS; CHORIONIC VILLI SAMPLING; CHROMOSOMES, HUMAN, PAIR 15; DNA; FEMALE; GESTATIONAL AGE; HUMANS; MOSAICISM; PRADER-WILLI SYNDROME; PREGNANCY; PRENATAL DIAGNOSIS; PROSPECTIVE STUDIES; TRISOMY;

EID: 0030815999     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1097-0223(199708)17:8<780::AID-PD133>3.0.CO;2-Z     Document Type: Article

References (9)

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