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Molecular study of three cases of odontohypophosphatasia resulting from heterozygosity for mutations in the tissue non-specific alkaline phosphatase gene.
Herasse M, Spentchian M, Taillandier A, Keppler-Noreuil K, Fliorito AN, Bergoffen J, Wallerstein R, Muti C, Simon-Bouy B, Mornet E. Herasse M, et al. Among authors: wallerstein r. J Med Genet. 2003 Aug;40(8):605-9. doi: 10.1136/jmg.40.8.605. J Med Genet. 2003. PMID: 12920074 Free PMC article. No abstract available.
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.
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.
Rubinstein-Taybi syndrome and hypoplastic left heart.
Hanauer D, Argilla M, Wallerstein R. Hanauer D, et al. Among authors: wallerstein r. Am J Med Genet. 2002 Sep 15;112(1):109-11. doi: 10.1002/ajmg.10617. Am J Med Genet. 2002. PMID: 12239733 No abstract available.
Maternal uniparental disomy of chromosome 16 and body stalk anomaly.
Chan Y, Silverman N, Jackson L, Wapner R, Wallerstein R. Chan Y, et al. Among authors: wallerstein r. Am J Med Genet. 2000 Oct 2;94(4):284-6. doi: 10.1002/1096-8628(20001002)94:4<284::aid-ajmg4>3.0.co;2-m. Am J Med Genet. 2000. PMID: 11038440
230 results