Comprehensive 4-year follow-up on a case of maternal heterodisomy for chromosome 16

American Journal of Medical Genetics

Volumn 66, Issue 2, 1996, Pages 204-208

  Schneider, Adele S ^a   Bischoff, Farideh Z ^c   McCaskill, Christopher ^c   Coady, Mary Luz ^b   Stopfer, Jill E ^a   Shaffer, Lisa G ^c  

^a ALBERT EINSTEIN MEDICAL CENTER   (United States)

^b ST CHRISTOPHER'S HOSPITAL FOR CHILDREN   (United States)

^c BAYLOR COLLEGE OF MEDICINE   (United States)

Author keywords

chromosome 16; confined placental mosaicism (CPM); intrauterine growth retardation (IUGR); short stature; uniparental disomy (UPD)

Indexed keywords

ADULT; AMNIOCENTESIS; ARTICLE; CASE REPORT; CHROMOSOME 16; DISOMY; FETUS DEATH; GENETIC ANALYSIS; HUMAN; HUMAN TISSUE; INTRAUTERINE GROWTH RETARDATION; MALE; PRIORITY JOURNAL; SHORT STATURE;

ABNORMALITIES, MULTIPLE; CHILD, PRESCHOOL; CHORIONIC VILLI SAMPLING; CHROMOSOME ABERRATIONS; CHROMOSOME DISORDERS; CHROMOSOMES, HUMAN, PAIR 16; FEMALE; FETAL GROWTH RETARDATION; FOLLOW-UP STUDIES; HUMANS; INFANT, NEWBORN; INFANT, SMALL FOR GESTATIONAL AGE; MALE; PREGNANCY; PREGNANCY COMPLICATIONS;

EID: 0030472329     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19961211)66:2<204::AID-AJMG16>3.0.CO;2-X     Document Type: Article

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