Prenatal diagnosis and carrier detection for glycogen storage disease type III using polymorphic DNA markers

Prenatal Diagnosis

Volumn 18, Issue 1, 1998, Pages 61-64

  Shen, Jianjun ^a   Liu, Hui Ming ^a   Mcconkie Rosell, Allyn ^a   Chen, Yuan Tsong ^a  

^a DUKE UNIVERSITY MEDICAL CENTER   (United States)

Author keywords

Carrier detection; Glycogen debranching enzyme; Glycogen storage disease type III; Polymorphic markers; Prenatal diagnosis

Indexed keywords

DNA MARKER; GLYCOGEN DEBRANCHING ENZYME;

ARTICLE; CONTROLLED STUDY; DNA POLYMORPHISM; FEMALE; FETUS; GENE MUTATION; GLYCOGEN STORAGE DISEASE TYPE 3; HETEROZYGOTE DETECTION; HUMAN; HUMAN CELL; MALE; POLYMERASE CHAIN REACTION; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; RESTRICTION MAPPING;

ADOLESCENT; AMNIOCENTESIS; CELLS, CULTURED; CHILD, PRESCHOOL; DNA; FEMALE; GENETIC MARKERS; GESTATIONAL AGE; GLYCOGEN STORAGE DISEASE TYPE III; HETEROZYGOTE DETECTION; HUMANS; POLYMERASE CHAIN REACTION; POLYMORPHISM, RESTRICTION FRAGMENT LENGTH; PREGNANCY; PRENATAL DIAGNOSIS;

EID: 0031974240     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1097-0223(199801)18:1<61::AID-PD223>3.0.CO;2-I     Document Type: Article

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