Prenatal diagnosis of a de novo trisomy 6q22.2 → 6qter and monosomy 1pter → 1p36.3. Case report with a 2-year follow-up and a brief review of other prenatal cases of partial trisomy 6q

Clinical Genetics

Volumn 51, Issue 2, 1997, Pages 115-117

  Kulharya, Anita S ^a   Carlin, Mary E ^b,c   Stettler, William A ^d   Huslig, Martine ^d   Kukolich, Mary K ^e   Garcia Heras, Jaime ^f  

^a MEDICAL COLLEGE OF GEORGIA   (United States)

^b Department of Orthopaedic Surgery   (United States)

^c Genetic Devmtl Ctr of the SW ^*  (United States)

^d Texas Maternal Fetal Medicine   (United States)

^e The Jane and John Justin Neuroscience Center   (United States)

^f TEXAS DEPARTMENT OF STATE HEALTH SERVICES   (United States)

Author keywords

Monosomy 1p; Partial trisomy 6q; Prenatal diagnosis

Indexed keywords

ARTICLE; BOY; CASE REPORT; FLUORESCENCE IN SITU HYBRIDIZATION; FOLLOW UP; HEART SURGERY; HUMAN; MALE; MONOSOMY; MORTALITY; PARTIAL TRISOMY; PRENATAL DIAGNOSIS; PRESCHOOL CHILD; PRIORITY JOURNAL; TRISOMY;

EID: 0030971229     PISSN: 00099163     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1399-0004.1997.tb02431.x     Document Type: Article

References (11)

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