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Radiology|March 1, 1991
Primary CT diagnosis of abdominal masses in a PACS environmentW H Straub, D Gur, W F Good, et al.
Molecular Genetics & Genomic Medicine|October 6, 2015
Regulatory variant in FZD6 gene contributes to nonsyndromic cleft lip and palate in an African-American familyNevena Cvjetkovic, Lorena Maili, Katelyn S Weymouth, et al.
Human Molecular Genetics|July 10, 2007
CRISPLD2: a novel NSCLP candidate geneBrett T Chiquet, Andrew C Lidral, Samuel Stal, et al.
American Journal of Medical Genetics. Part A|April 18, 2018
Soft tissue nasal asymmetry as an indicator of orofacial cleft predispositionCharles Zhang, Steven F Miller, Jasmien Roosenboom, et al.
American Journal of Human Genetics|August 1, 1995
Refinement of the multiple exostoses locus (EXT2) to a 3-cM interval on chromosome 11W Wuyts, S Ramlakhan, W Van Hul, et al.
American Journal of Medical Genetics. Part A|August 12, 2011
Variants in genes that encode muscle contractile proteins influence risk for isolated clubfootKatelyn S Weymouth, Susan H Blanton, Michael J Bamshad, et al.
American Journal of Human Genetics|April 1, 1996
Delineation of a contiguous gene syndrome with multiple exostoses, enlarged parietal foramina, craniofacial dysostosis, and mental retardation, caused by deletions in the short arm of chromosome 11O Bartsch, W Wuyts, W Van Hul, et al.
Plos Genetics|October 8, 2013
A GDF5 point mutation strikes twice--causing BDA1 and SYNS2Elisa Degenkolbe, Jana König, Julia Zimmer, et al.
Medrxiv : the Preprint Server for Health Sciences|February 17, 2023
Rare variants found in multiplex families with orofacial clefts: Does expanding the phenotype make a difference?Kimberly K Diaz Perez, Sydney Chung, S Taylor Head, et al.
Blood|November 2, 2002
IL-7 therapy dramatically alters peripheral T-cell homeostasis in normal and SIV-infected nonhuman primatesTerry J Fry, Marcin Moniuszko, Stephen Creekmore, et al.
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