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American Journal of Medical Genetics|September 1, 1983
Probable autosomal recessive inheritance of polysplenia, situs inversus and cardiac defects in an Amish familyG L Arnold, D Bixler, D GirodAmerican Journal of Medical Genetics|September 1, 1983
Possible new autosomal recessive syndrome with unusual renal histopathological changesJ E Allanson, J T Pantzar, P M MacLeodAmerican Journal of Medical Genetics|September 1, 1983
Parents' adaptation to early diagnosis of sex chromosome anomaliesM H Puck, B G Bender, J B Borelli, et al.American Journal of Medical Genetics|October 1, 1983
The Weissenbacher-Zweymüller, Stickler, and Marshall syndromes: further evidence for their identityR M Winter, M Baraitser, K M Laurence, et al.American Journal of Medical Genetics|April 1, 1982
Occurrence of cyclopia, myelomeningocele, deafness, and abducens paralysis in siblingsU Burck, K R Held, H J KitschkeAmerican Journal of Medical Genetics|January 1, 1981
Neurofibromatosis in monozygotic twins: a case report of spontaneous mutationA J Vaughn, D Bachman, A SommerAmerican Journal of Medical Genetics|January 1, 1981
Familial cutaneous amyloidosis with systemic manifestations in malesM W Partington, P J Marriott, R S Prentice, et al.American Journal of Medical Genetics|January 1, 1983
Duplication 10p in a girl due to a maternal translocation t(10;14) (p11:p12)C H Gonzalez, A E Billerbeck, L C Takayama, et al.American Journal of Medical Genetics|January 1, 1983
Identical multiple congenital anomalies/mental retardation (MCA/MR) syndrome due to del(2)(q32) in two sisters with intrachromosomal insertional translocation in their fatherG S Pai, J F Rogers, A SommerAmerican Journal of Medical Genetics|January 1, 1983
Pachyonychia Congenita (Jadassohn-Lewandowsky syndrome): a seventeen-member, four-generation pedigree with unusual respiratory and dental involvementJ B Stieglitz, W R CenterwallPageof 854