- Title
- GPSM2 Mutations in Chudley―McCullough Syndrome
- Creators
- Oscar DIAZ-HORTA - Department of Human Genetics, Miller School of Medicine, University of Miami, Miami, Florida, United StatesAsli SIRMACI - Department of Human Genetics, Miller School of Medicine, University of Miami, Miami, Florida, United StatesDan DOHERTY - Department of Pediatrics, University of Washington and Seattle Children's Hospital, Seattle, Washington, United StatesWalter NANCE - Department of Human and Molecular Genetics, Virginia, Commonwealth University, Richmond, Virginia, United StatesKathleen AMOS - Department of Biology, Gallaudet University, Washington, District of Columbia, United StatesArti PANDYA - Department of Human and Molecular Genetics, Virginia, Commonwealth University, Richmond, Virginia, United StatesMustafa TEKIN - Department of Human Genetics, Miller School of Medicine, University of Miami, Miami, Florida, United States
- Publication Details
- American journal of medical genetics. Part A, Vol.158(11), pp.2972-2973
- Publisher
- Wiley-Liss; Chichester
- Academic Unit
- Miller School of Medicine; UMMG Dept of Human Genetics - Clinical and Translational Genetics; UMMG Dept of Human Genetics (Dr. John T. Macdonald Foundation)
- Language
- English
- Resource Type
- Journal article
- PMID
- 22987632
- PMCID
- PMC3657751
- Record Identifier
- 991031578683402976
Journal article
GPSM2 Mutations in Chudley―McCullough Syndrome
American journal of medical genetics. Part A, Vol.158(11), pp.2972-2973
2012
PMCID: PMC3657751
PMID: 22987632
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13 Record Views
InCites Highlights
These are selected metrics from InCites Benchmarking & Analytics tool, related to this output
- Collaboration types
- Domestic collaboration
- Citation topics
- 1 Clinical & Life Sciences
- 1.257 Birth defects
- 1.257.983 Hydrocephalus
- Web Of Science research areas
- Genetics & Heredity
- ESI research areas
- Molecular Biology & Genetics
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Source: InCites