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American Journal of Medical Genetics|October 1, 1987
Sudden death in childhood in a case of the G syndromeS L Einfeld, M J Fairley, B F Green, et al.European Journal of Pediatrics|February 21, 1977
Hemihypotrophy in a girl with a translocation t(13q;7p)F A Marçallo, L C Werneck, R F Pilotto, et al.American Journal of Medical Genetics|September 1, 1984
The Perlman syndrome: familial renal dysplasia with Wilms tumor, fetal gigantism and multiple congenital anomaliesG Neri, M E Martini-Neri, B E Katz, et al.Human Genetics|December 1, 1986
Severe short-limb dwarfism resembling Grebe chondrodysplasiaA S Teebi, S A Al-Awadi, J M Opitz, et al.European Journal of Pediatrics|April 6, 1976
Studies of malformation syndromes of man XXXXIA: anatomical studies in the Hanhart syndrome--a pathogenetic hypothesisE T Bersu, J C Pettersen, W J Charboneau, et al.American Journal of Medical Genetics|February 1, 1982
Phenotypic effects of inherited balanced translocationZ Ying, C Zaiyu, L Chunyun, et al.American Journal of Medical Genetics|August 1, 1985
An X-linked recessive basal ganglia disorder with mental retardationR Laxova, E S Brown, K Hogan, et al.American Journal of Medical Genetics|July 27, 2001
Evidence for the "midline" hypothesis in associated defects of laterality formation and multiple midline anomaliesE Gilbert-Barness, D Debich-Spicer, M M Cohen, et al.American Journal of Medical Genetics. Supplement|January 1, 1986
Two sporadic cases of amelia/phocomelia with similar phenotype: rare and unusually symmetrical form of FFU dysostosis or separate entity?N B Kardon, L P Dana, J M FitzGerald, et al.Human Molecular Genetics|August 11, 1999
Subcortical band heterotopia in rare affected males can be caused by missense mutations in DCX (XLIS) or LIS1D T Pilz, J Kuc, N Matsumoto, et al.Pageof 40