Showing results (171-180 of 262) with videos related to
Sort By:
Pageof 27
American Journal of Medical Genetics|October 1, 1991
Syndrome of mental retardation and distal arthrogryposis in sibsD Chitayat, K A Hodgkinson, S Blaichman, et al.Regulatory Peptides|November 5, 1998
Endogenous neuropeptide Y mediates vasoconstriction during endotoxic and hemorrhagic shockN U Qureshi, E K Dayao, S Shirali, et al.Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|May 23, 2019
Microarray and RASopathy-disorder testing in fetuses with increased nuchal translucencyP Sinajon, D Chitayat, M Roifman, et al.Clinical Genetics|May 28, 2014
Fetal skeletal dysplasias in a tertiary care center: radiology, pathology, and molecular analysis of 112 casesE Barkova, U Mohan, D Chitayat, et al.Clinical Genetics|April 5, 2014
Hypotrichosis-lymphedema-telangiectasia-renal defect associated with a truncating mutation in the SOX18 geneS Moalem, P Brouillard, D Kuypers, et al.Journal of Inherited Metabolic Disease|January 1, 1987
Elevation of serum beta-hexosaminidase and alpha-D-mannosidase in type 2 Gaucher disease: a clinical and biochemical studyD Chitayat, S Nakagawa, R W Marion, et al.Neurofibromatosis|January 1, 1989
Encephalocraniocutaneous lipomatosis. Report of two cases and a review of the literatureJ S Bamforth, V M Riccardi, P Thisen, et al.American Journal of Human Genetics|February 11, 1999
Brachydactyly type B: clinical description, genetic mapping to chromosome 9q, and evidence for a shared ancestral mutationY Gong, D Chitayat, B Kerr, et al.The Journal of Pediatrics|July 1, 1992
Brain dysgenesis and congenital intracerebral calcification associated with 3-hydroxyisobutyric aciduriaD Chitayat, K Meagher-Villemure, O A Mamer, et al.Critical Care Medicine|July 1, 1991
Immune dysfunction in children after corrective surgery for congenital heart diseaseG J Hauser, M M Chan, W F Casey, et al.Pageof 27