Rare Trisomy Mosaicism Diagnosed in Amniocytes, Involving an Autosome Other Than Chromosomes 13, 18, 20, and 21: Karyotype/phenotype Correlations
Year: 1997
Type: article
Study design: Observational Study
Source: Prenatal Diagnosis
Authors: LILLIAN Y. F. HSU, MING-TSUNG YU, RICHARD L. NEU, DANIEL L. VAN DYKE, PETER A. BENN, CHRISTY L. BRADSHAW, LISA G. SHAFFER, RODNEY R. HIGGINS, GABRIEL S. KHODR, CYNTHIA C. MORTON, HUNGSHU WANG, ARTHUR R. BROTHMAN, DIANNE CHADWICK, CHRISTINE M. DISTECHE, LAUREN S. JENKINS, DAGMAR K. KALOUSEK, TAPIO J. PANTZAR, PHILIP WYATT
Institutions: New York University, Henry Ford Hospital, UConn Health, University of California San Diego, Baylor College of Medicine, Brigham and Women's Hospital, Children's Hospital of Eastern Ontario, University of Utah, Credit Valley Hospital, University of Washington, Kaiser Permanente San Jose Medical Center, University of British Columbia, BC Children's Hospital, North York General Hospital
Language: English
Field: Medicine
Domain: Health Sciences
Open Access status: closed
OpenAlex ID: W2065226010