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American Journal of Medical Genetics|March 1, 1993
Autosomal dominant multiple café-au-lait spots and neurofibromatosis-1: evidence of non-linkageJ Charrow, R Listernick, K WardAmerican Journal of Medical Genetics|March 1, 1993
Complications in the genotypic molecular diagnosis of pseudo arylsulfatase A deficiencyN Shen, Z G Li, J S Waye, et al.American Journal of Medical Genetics|March 1, 1993
New X-linked syndrome with severe mental retardation, severely impaired vision, severe hearing defect, epileptic seizures, spasticity, restricted joint mobility, and early deathK H Gustavson, G Annerén, H Malmgren, et al.American Journal of Medical Genetics|March 15, 1993
Multiple craniofacial anomalies associated with an interstitial deletion of chromosome 1(q21->q25)L G Leichtman, D Strum, A R BrothmanAmerican Journal of Medical Genetics|March 15, 1993
Spastic paraplegia, epilepsy, and mental retardation in several members of a family: a novel genetic disorderG L Gigli, M Diomedi, G Bernardi, et al.American Journal of Medical Genetics|March 15, 1993
Balanced reciprocal translocation mosaicism associated with an abnormal phenotypeD J Aughton, A A AlSaadi, A I Canady, et al.American Journal of Medical Genetics|March 15, 1993
Visceral anomalies in the Apert syndromeM M Cohen, S KreiborgAmerican Journal of Medical Genetics|February 15, 1993
Aase syndrome: novel radiographic featuresA V Hing, S B DowtonAmerican Journal of Medical Genetics|February 15, 1993
Segregation analysis of hypospadias: a reanalysis of published pedigree dataE L Harris, T H BeatyAmerican Journal of Medical Genetics|February 15, 1993
Photoanthropometric study of facial growth in Noonan syndromeM Sharland, M Morgan, M A PattonPageof 854