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The spectrum of mutations in TBX3: Genotype/Phenotype relationship in ulnar-mammary syndrome.
Bamshad M, Le T, Watkins WS, Dixon ME, Kramer BE, Roeder AD, Carey JC, Root S, Schinzel A, Van Maldergem L, Gardner RJ, Lin RC, Seidman CE, Seidman JG, Wallerstein R, Moran E, Sutphen R, Campbell CE, Jorde LB. Bamshad M, et al. Among authors: wallerstein r. Am J Hum Genet. 1999 Jun;64(6):1550-62. doi: 10.1086/302417. Am J Hum Genet. 1999. PMID: 10330342 Free PMC article.
Short rib-polydactyly syndrome: more evidence of a continuous spectrum.
Sarafoglou K, Funai EF, Fefferman N, Zajac L, Geneiser N, Paidas MJ, Greco A, Wallerstein R. Sarafoglou K, et al. Among authors: wallerstein r. Clin Genet. 1999 Aug;56(2):145-8. doi: 10.1034/j.1399-0004.1999.560209.x. Clin Genet. 1999. PMID: 10517252
Early prenatal ultrasound diagnosis of cleidocranial dysplasia.
Stewart PA, Wallerstein R, Moran E, Lee MJ. Stewart PA, et al. Among authors: wallerstein r. Ultrasound Obstet Gynecol. 2000 Feb;15(2):154-6. doi: 10.1046/j.1469-0705.2000.00041.x. Ultrasound Obstet Gynecol. 2000. PMID: 10776001 Free article.
Mutation analysis of B3GALTL in Peters Plus syndrome.
Reis LM, Tyler RC, Abdul-Rahman O, Trapane P, Wallerstein R, Broome D, Hoffman J, Khan A, Paradiso C, Ron N, Bergner A, Semina EV. Reis LM, et al. Among authors: wallerstein r. Am J Med Genet A. 2008 Oct 15;146A(20):2603-10. doi: 10.1002/ajmg.a.32498. Am J Med Genet A. 2008. PMID: 18798333 Free PMC article.
Lateral meningocele syndrome: three new patients and review of the literature.
Gripp KW, Scott CI Jr, Hughes HE, Wallerstein R, Nicholson L, States L, Bason LD, Kaplan P, Zderic SA, Duhaime AC, Miller F, Magnusson MR, Zackai EH. Gripp KW, et al. Among authors: wallerstein r. Am J Med Genet. 1997 Jun 13;70(3):229-39. Am J Med Genet. 1997. PMID: 9188658 Review.
Diagnostic analysis of the Rubinstein-Taybi syndrome: five cosmids should be used for microdeletion detection and low number of protein truncating mutations.
Petrij F, Dauwerse HG, Blough RI, Giles RH, van der Smagt JJ, Wallerstein R, Maaswinkel-Mooy PD, van Karnebeek CD, van Ommen GJ, van Haeringen A, Rubinstein JH, Saal HM, Hennekam RC, Peters DJ, Breuning MH. Petrij F, et al. Among authors: wallerstein r. J Med Genet. 2000 Mar;37(3):168-76. doi: 10.1136/jmg.37.3.168. J Med Genet. 2000. PMID: 10699051 Free PMC article.
229 results