Rare trisomy mosaicism diagnosed in amniocytes, involving an autosome other than chromosomes 13, 18, 20, and 21: Karyotype/phenotype correlations

Prenatal Diagnosis

Volumn 17, Issue 3, 1997, Pages 201-242

  Hsu, Lillian Y F ^a,b,s   Yu, Ming Tsung ^a   Neu, Richard L ^c   Van Dyke, Daniel L ^d   Benn, Peter A ^e   Bradshaw, Christy L ^f   Shaffer, Lisa G ^g   Higgins, Rodney R ^h   Khodr, Gabriel S ⁱ   Morton, Cynthia C ^j   Wang, Hungshu ^k   Brothman, Arthur R ^l   Chadwick, Dianne ^m   Disteche, Christine M ⁿ   Jenkins, Lauren S ^o   Kalousek, Dagmar K ^p   Pantzar, Tapio J ^q   Wyatt, Philip ^r  

^a Prenatal Diagn Lab New York City   (United States)

^b NEW YORK UNIVERSITY SCHOOL OF MEDICINE   (United States)

^c GENZYME GENETICS   (United States)

^d HENRY FORD HOSPITAL   (United States)

^e UNIVERSITY OF CONNECTICUT HEALTH CENTER   (United States)

^f UNIVERSITY OF CALIFORNIA   (United States)

^g BAYLOR COLLEGE OF MEDICINE   (United States)

^h Allina Hospitals & Clinics   (United States)

ⁱ Southwest Genetics   (United States)

^j BRIGHAM AND WOMEN S HOSPITAL   (United States)

^k CHILDREN S HOSPITAL OF EASTERN ONTARIO   (Canada)

^l UNIVERSITY OF UTAH SCHOOL OF MEDICINE   (United States)

^m CREDIT VALLEY HOSPITAL   (Canada)

ⁿ UNIVERSITY OF WASHINGTON   (United States)

^o Department of Genetics   (United States)

^p UNIVERSITY OF BRITISH COLUMBIA   (Canada)

^q BC CHILDREN S HOSPITAL   (Canada)

^r NORTH YORK GENERAL HOSPITAL   (Canada)

^s Prenatal Diagn Lab New York City   (United States)

more..

Author keywords

Amniocytes; Prenatal cytogenetic diagnosis; Rare trisomy mosaicism

Indexed keywords

AMNIOCENTESIS; AMNION CELL; ARTICLE; AUTOSOME MOSAICISM; BIRTH; CHROMOSOME 11; CHROMOSOME 13; CHROMOSOME 14; CHROMOSOME 15; CHROMOSOME 16; CHROMOSOME 18; CHROMOSOME 2; CHROMOSOME 20; CHROMOSOME 21; CHROMOSOME 7; CYTOGENETICS; DNA DETERMINATION; FETUS; FIBROBLAST; GENOME IMPRINTING; HUMAN; HUMAN CELL; KARYOTYPE; MAJOR CLINICAL STUDY; NEWBORN; PHENOTYPE; PLACENTA; PREGNANCY; PREGNANCY TERMINATION; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; RISK; TRISOMY; ULTRASOUND;

ADOLESCENT; ADULT; AMNIOCENTESIS; AMNIOTIC FLUID; CHROMOSOME ABERRATIONS; CHROMOSOME DISORDERS; FEMALE; HUMANS; KARYOTYPING; MALE; MIDDLE AGED; MOSAICISM; PHENOTYPE; PREGNANCY; PREGNANCY OUTCOME; TRISOMY;

EID: 0030973681     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1097-0223(199703)17:3<201::AID-PD56>3.0.CO;2-H     Document Type: Article

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