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American Journal of Medical Genetics|February 1, 1991
X-linked mental retardation with marfanoid habitus: first report of four Italian patientsF Lalatta, E Livini, A Selicorni, et al.American Journal of Medical Genetics|February 1, 1991
Fragile X families in a northern Swedish county: a genealogical study of possibly affected individuals in the nineteenth centuryU Drugge, H K Blomquist, K H Gustavson, et al.American Journal of Medical Genetics|June 1, 1989
Familial distal arthrogryposis with craniofacial abnormalities: a new subtype of type II?C A Moore, D D WeaverAmerican Journal of Medical Genetics|June 1, 1989
Clinical, pathological, and biochemical studies on an infantile case of sulfatide/GM1 activator protein deficiencyD A Wenger, G DeGala, C Williams, et al.American Journal of Medical Genetics|October 1, 1988
Hyperpigmented lesions of the retinal pigment epithelium in familial adenomatous polyposisR H Baker, M H Heinemann, H H Miller, et al.American Journal of Medical Genetics|February 1, 1985
Deletions of proximal 15q and non-classical Prader-Willi syndrome phenotypesS Schwartz, S R Max, S R Panny, et al.American Journal of Medical Genetics|February 1, 1991
Relationship between age and IQ among fragile X males: a multicenter studyG S Fisch, T Arinami, U Froster-Iskenius, et al.American Journal of Medical Genetics|February 1, 1991
Short-term memory and cognitive variability in adult fragile X femalesR de von Flindt, B Bybel, A E Chudley, et al.American Journal of Medical Genetics|July 1, 1994
Seckel syndrome in a Yemeni family in Saudi ArabiaA G Krishna, E M Scrimgeour, T H ZawawiAmerican Journal of Medical Genetics|July 1, 1994
Oral-facial-digital syndrome with retinal abnormalities: OFDS type IX. A further case reportN C Nevin, J Silvestri, D C Kernohan, et al.Pageof 854