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Journal of Medical Genetics|December 1, 1977
A 'new' syndrome of mental retardation with characteristic facies and brachyphalangyA G Hunter, P J McAlpine, N L Rudd, et al.Journal of Medical Genetics|August 1, 1979
Night blindness, characteristic facies, and skeletal abnormalities in two brothersA G Hunter, D R Thompson, M H Reed, et al.Journal of Gastrointestinal Surgery : Official Journal of the Society for Surgery of the Alimentary Tract|February 28, 2014
The incidence of hiatal hernia after minimally invasive esophagectomyNathan W Bronson, Renato A Luna, John G Hunter, et al.Frontiers in Behavioral Neuroscience|July 25, 2022
The Role of Transposable Elements in Sexual DevelopmentVic Shao-Chih Chiang, Holly DeRosa, Jin Ho Park, et al.American Journal of Human Genetics|January 1, 1989
Linkage analysis of the apolipoprotein C2 gene and myotonic dystrophy on human chromosome 19 reveals linkage disequilibrium in a French-Canadian populationA E MacKenzie, H L MacLeod, A G Hunter, et al.Molecular and Cellular Endocrinology|January 1, 1982
The functional activity of adult mouse Leydig cells in monolayer culture. Effect of lutropin and foetal calf serumM G Hunter, R Magee-Brown, C J Dix, et al.Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|December 26, 2001
Long-term outcome of uncomplicated infantile exotropiaD G Hunter, J B Kelly, A N Buffenn, et al.The American Journal of Clinical Nutrition|March 1, 1996
Cross-calibration of body-composition techniques against dual-energy X-ray absorptiometry in young childrenM I Goran, P Driscoll, R Johnson, et al.European Journal of Medical Genetics|December 29, 2010
Diagnosis of distal 22q11.2 deletion syndrome in a patient with a teratoid/rhabdoid tumourR A Beddow, M Smith, A Kidd, et al.Clinical Genetics|December 1, 1982
Two children with deletion of the long arm of chromosome 4 with breakpoint at band q33D J Tomkins, A G Hunter, I A Uchida, et al.Pageof 97