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American Journal of Medical Genetics|February 5, 1998
Karsch-Neugebauer syndrome in two sibs with unaffected parentsS C Wong, J M Cobben, S Hiemstra, et al.American Journal of Medical Genetics|February 5, 1998
Syndromal and nonsyndromal primary trigonocephaly: analysis of a series of 237 patientsE Lajeunie, M Le Merrer, D Marchac, et al.American Journal of Medical Genetics|April 17, 1998
Sweat electrolyte and cystic fibrosis mutation analysis allows early diagnosis in Brazilian children with clinical signs compatible with cystic fibrosisE Rabbi-Bortolini, A L Bernardino, A L Lopes, et al.American Journal of Medical Genetics|April 17, 1998
Correlated heart/limb anomalies in Mendelian syndromes provide evidence for a cardiomelic developmental fieldG N WilsonAmerican Journal of Medical Genetics|April 17, 1998
Complex familial rearrangement of chromosome 9p24.3 detected by FISHG M Repetto, J Wagstaff, B R Korf, et al.American Journal of Medical Genetics|November 1, 1985
Morquio syndrome (MPS IVA) and hypophosphatasia in a Hutterite kindredR B Lowry, F F Snyder, R L Wesenberg, et al.American Journal of Medical Genetics|November 1, 1985
Neurofibromatosis and fragile-X syndrome in the same patientJ A Mitchell, J Wray, K MichalskiAmerican Journal of Medical Genetics|November 1, 1988
Evidence for autosomal recessive inheritance of progeria (Hutchinson Gilford)A T MacielAmerican Journal of Medical Genetics|December 1, 1988
Recurrence risks for relatives in families with an isolated case of the fragile X syndromeS L Sherman, A Rogatko, G TurnerAmerican Journal of Medical Genetics|December 1, 1988
The use of early simultaneous percutaneous umbilical blood sampling (PUBS) and amniocentesis for prenatal fragile X chromosome diagnosisM G Butler, V G Dev, D Shah, et al.Pageof 854