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American Journal of Medical Genetics|November 15, 1992
New oral-acral syndrome with partial agenesis of the maxillary bonesA Verloes, L KoulischerAmerican Journal of Medical Genetics|November 15, 1992
Dietary folate and nonneural midline birth defects: no evidence of an association from a case-control study in Western AustraliaC Bower, F J StanleyAmerican Journal of Medical Genetics|November 25, 1992
Spondylometaphyseal dysplasia, Sedaghatian typeJ N Peeden, D L Rimoin, R S Lachman, et al.American Journal of Medical Genetics|November 15, 1992
Double-blind, placebo-controlled crossover study of folinic acid (Leucovorin for the treatment of fragile X syndromeC M Strom, R M Brusca, W J PizziAmerican Journal of Medical Genetics|December 1, 1992
Late diagnosis of phenylketonuria in a Bedouin motherR Usha, R Uma, T I Farag, et al.American Journal of Medical Genetics|December 11, 1992
Dominant mesomelic dysplasia, ankle, carpal, and tarsal synostosis type: a new autosomal dominant bone disorderP N Kantaputra, R J Gorlin, L O LangerAmerican Journal of Medical Genetics|December 1, 1992
Choanal atresia: evidence for autosomal recessive inheritanceR Gershoni-BaruchAmerican Journal of Medical Genetics|December 1, 1992
New hereditary malformation syndrome of unusual facial appearance, skeletal deformities, and musculoskeletal and sensory defectsL T Middleton, V Anastasiades, K Panayidou, et al.American Journal of Medical Genetics|December 1, 1992
Upper limb deficiencies and associated malformations: a population-based studyU G Froster, P A BairdAmerican Journal of Medical Genetics|December 1, 1992
Chondrodysplasia punctata: another possible X-linked recessive caseC P Bennett, A C Berry, D J Maxwell, et al.Pageof 854