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American Journal of Medical Genetics|January 1, 1986
Fra(2) (q13) and inv(9) (p11q12) in autism: causal relationship?P Jayakar, A E Chudley, M Ray, et al.American Journal of Medical Genetics|January 1, 1986
Fragile X chromosome frequency is consistent temporally and within replicate culturesE C Jenkins, B R Kastin, M S Krawczun, et al.American Journal of Medical Genetics|January 1, 1986
Sex chromosome aneuploidy in fragile X carriersK B NielsenAmerican Journal of Medical Genetics|January 1, 1986
Studies of the fragile (X) syndrome in populations of mentally retarded individuals in HawaiiP A Jacobs, M Mayer, M A AbruzzoAmerican Journal of Medical Genetics|January 1, 1986
Population incidence and segregation ratios in the Martin-Bell syndromeT P Webb, S E Bundey, A I Thake, et al.American Journal of Medical Genetics|March 1, 1986
Trisomy 22 mosaicism syndrome and Ullrich-Turner stigmataW Wertelecki, W R Breg, J M Graham, et al.American Journal of Medical Genetics|January 1, 1987
The Johanson-Blizzard syndrome: a second report of full autopsy findingsJ B Moeschler, M J Polak, J J Jenkins, et al.American Journal of Medical Genetics|January 1, 1987
Mosaic trisomy 7 and renal dysplasiaM S Verp, A P Amarose, J R Esterly, et al.American Journal of Medical Genetics|January 1, 1987
Autosomal dominant painful plantar callositiesA Rachid, N Freire-Maia, M PinheiroAmerican Journal of Medical Genetics|January 1, 1987
DOOR syndrome (deafness, onycho-osteodystrophy, and mental retardation): elevated plasma and urinary 2-oxoglutarate in three unrelated patientsM A Patton, S Krywawych, R M Winter, et al.Pageof 854