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Journal of Medical Genetics|August 1, 1989
Familial translocation t(9;16)C Dowman, D Lockwood, J AllansonAmerican Journal of Human Genetics|March 1, 1990
A genetic study of Hirschsprung diseaseJ A Badner, W K Sieber, K L Garver, et al.Journal of Neurology, Neurosurgery, and Psychiatry|August 20, 2002
Characteristics of patients with persistent severe disability and medically unexplained neurological symptoms: a pilot studyJ Allanson, C Bass, D T WadeEnzyme|January 1, 1980
Origin of lactate dehydrogenase in amniotic fluidK L Garver, S G Marchese, A E Wineman, et al.Genetic Testing|January 1, 1997
Prenatal diagnosis in congenital contractural arachnodactylyS Belleh, L Spooner, J Allanson, et al.Journal of Medical Genetics|July 1, 1989
Severe Silver-Russell syndromeD Donnai, E Thompson, J Allanson, et al.Journal of Medical Genetics|November 1, 1989
Abnormal chromosome complement resulting from a familial inversion of chromosome 2S Richter, B Lockwood, D Lockwood, et al.Clinical Genetics|April 1, 1981
Increased amnionic fluid alpha-fetoprotein due to a holoacardium amorphous twinJ H Harger, N Doshi, S Marchese, et al.Human Genetics|October 1, 1989
Not all chromosome imbalance resulting from the 11q;22q translocation is due to 3:1 segregation in first meiosisD H Lockwood, A Farrier, F Hecht, et al.Clinical Genetics|November 1, 1977
Meiotic consequences of an intrachromosomal insertion of chromosome No 1: a family pedigreeS F Pan, S R Fatora, R Sorg, et al.Pageof 9