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Smith-Lemli-Opitz syndrome in an inbred family.
Nevo S, Benderly A, Levy J, Katznelson MB. Nevo S, et al. Among authors: katznelson mb. Am J Dis Child. 1972 Sep;124(3):431-3. doi: 10.1001/archpedi.1972.02110150129021. Am J Dis Child. 1972. PMID: 5056882 No abstract available.
Acrocephalopolysyndactyly type IV: a new genetic syndrome in 3 sibs.
Goodman RM, Sternberg M, Shem-Tov Y, Katznelson MB, Hertz M, Rotem Y. Goodman RM, et al. Among authors: katznelson mb. Clin Genet. 1979 Mar;15(3):209-14. doi: 10.1111/j.1399-0004.1979.tb00969.x. Clin Genet. 1979. PMID: 421359 No abstract available.
The question of trisomy 22 syndrome.
Goodman RM, Katznelson MB, Spero M, Shaki R, Padeh B, Sadan N. Goodman RM, et al. Among authors: katznelson mb. J Pediatr. 1971 Jul;79(1):174-5. doi: 10.1016/s0022-3476(71)80096-3. J Pediatr. 1971. PMID: 5091263 No abstract available.
New form of postaxial acrofacial dysostosis?
Arens R, Reichman B, Katznelson MB, Goodman RM. Arens R, et al. Among authors: katznelson mb. Am J Med Genet. 1991 Dec 15;41(4):438-43. doi: 10.1002/ajmg.1320410411. Am J Med Genet. 1991. PMID: 1776633
42 results