Genotype and phenotype in 12 additional individuals with SATB2-associated syndrome.

Saved in:
Bibliographic Details
Title: Genotype and phenotype in 12 additional individuals with SATB2-associated syndrome.
Authors: Zarate YA; Section of Genetics and Metabolism, University of Arkansas for Medical Sciences, Little Rock, Arkansas., Kalsner L; Department of Pediatrics, Connecticut Children's Medical Center, Hartford, Connecticut., Basinger A; Department of Pediatrics, Cook Children's Physician Network, Fort Worth, Texas., Jones JR; Department of Genetics, Greenwood Genetic Center, Greenwood, South Carolina., Li C; Clinical Genetics program, McMaster University Medical Center, Hamilton, Ontario, Canada., Szybowska M; Clinical Genetics program, McMaster University Medical Center, Hamilton, Ontario, Canada., Xu ZL; Faculty of Health Sciences, McMaster University, Hamilton, Ontario, Canada., Vergano S; Division of Medical Genetics and Metabolism, Children's Hospital of The King's Daughters, Norfolk, Virginia., Caffrey AR; Health Outcomes, Collage of pharmacy, University of Rhode Island, Kingston, Rhode Island., Gonzalez CV; Biostatistics Program, Department of Pediatrics, University of Arkansas for Medical Sciences, Little Rock, Arkansas., Dubbs H; Department of Genetics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania., Zackai E; Department of Genetics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania., Millan F; Department of Molecular Genetics, GeneDx, Gaithersburg, Maryland., Telegrafi A; Department of Molecular Genetics, GeneDx, Gaithersburg, Maryland., Baskin B; Department of Molecular Genetics, GeneDx, Gaithersburg, Maryland., Person R; Department of Molecular Genetics, GeneDx, Gaithersburg, Maryland., Fish JL; Department of Biological Sciences, University of Massachusetts Lowell, Lowell, Massachusetts., Everman DB; Department of Genetics, Greenwood Genetic Center, Greenwood, South Carolina.
Source: Clinical genetics [Clin Genet] 2017 Oct; Vol. 92 (4), pp. 423-429. Date of Electronic Publication: 2017 Mar 07.
Publication Type: Journal Article
Journal Info: Publisher: Munksgaard Country of Publication: Denmark NLM ID: 0253664 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1399-0004 (Electronic) Linking ISSN: 00099163 NLM ISO Abbreviation: Clin Genet Subsets: MEDLINE
Database: MEDLINE Ultimate
Description
ISSN:1399-0004
DOI:10.1111/cge.12982