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American Journal of Medical Genetics|March 8, 2000
Interstitial tandem duplication of 6p: a case with partial trisomy (6)(p12p21.3)A Villa, E G Gomez, L Rodríguez, et al.American Journal of Medical Genetics|March 8, 2000
Fronto-otopalatodigital osteodysplasia: clinical evidence for a single entity encompassing Melnick-Needles syndrome, otopalatodigital syndrome types 1 and 2, and frontometaphyseal dysplasiaA Verloes, S Lesenfants, M Barr, et al.American Journal of Medical Genetics|August 18, 2000
Familial congenital pulmonary lymphangectasia, non-immune hydrops fetalis, facial and lower limb lymphedema: confirmation of Njolstad's reportS Jacquemont, S Barbarot, M Bocéno, et al.American Journal of Medical Genetics|August 18, 2000
Magnetic resonance findings and ophthalmologic abnormalities are correlated in patients with neurofibromatosis type 1 (NF1)M Sigorini, G Zuccoli, F Ferrozzi, et al.American Journal of Medical Genetics|August 18, 2000
Familial cryptic (20;21) translocation identified by in situ hybridization technologiesK A Leppig, S Ball, K Au, et al.American Journal of Medical Genetics|August 18, 2000
Missense mutation in PAK3, R67C, causes X-linked nonspecific mental retardationT Bienvenu, V des Portes, N McDonell, et al.American Journal of Medical Genetics|August 18, 2000
Clinical manifestations in a large hereditary hemorrhagic telangiectasia (HHT) type 2 kindredJ E McDonald, F J Miller, S E Hallam, et al.American Journal of Medical Genetics|April 6, 2000
Quantitative approach to identifying abnormal variation in the human face exemplified by a study of 278 individuals with five craniofacial syndromesR E Ward, P L Jamison, J E AllansonAmerican Journal of Medical Genetics|April 6, 2000
Fetomaternal cell trafficking: a new cause of disease?D W BianchiAmerican Journal of Medical Genetics|April 6, 2000
Familial hypercholesterolemia study in Sardinia using 6 LDLR polymorphic markers based on PCRS Orrù, S Pintor, A Loizedda, et al.Pageof 854