Prenatal testing for uniparental disomy (UPD) [2]

Prenatal Diagnosis

Volumn 21, Issue 6, 2001, Pages 513-

  Jay, Anne M ^a   Roberts, E ^a   Davies, T ^b   Barnes, I ^c   Curtis, M ^d   Healey, K ^e   Davison, E V ^a  

^a BIRMINGHAM WOMEN S HOSPITAL   (United Kingdom)

^b SOUTHMEAD HOSPITAL   (United Kingdom)

^c SHEFFIELD CHILDREN S HOSPITAL   (United Kingdom)

^d UNIVERSITY HOSPITAL OF WALES   (United Kingdom)

^e LEICESTER ROYAL INFIRMARY   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

CHROMOSOME MARKER; GENE TRANSLOCATION; HUMAN; LETTER; MOSAICISM; PHENOTYPE; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; SUPERNUMERARY CHROMOSOME; UNIPARENTAL DISOMY;

FEMALE; GENETIC SCREENING; HUMANS; PARENTS; PREGNANCY; PRENATAL DIAGNOSIS; TRANSLOCATION, GENETIC;

EID: 0034912678     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/pd.25     Document Type: Letter

References (3)

1. Prenatal UPD testing survey in Robertsonian translocations
2. Prospective prenatal diagnosis of Prader Willi syndrome due to maternal disomy for chromosome 15 following trisomic zygote rescue
3. Prenatal diagnosis of maternal heterodisomy 15 following detection of trisomy 15 mosaicism in amniotic fluid cell culture