Wallerstein R - Search Results

1

Dubowitz syndrome in a boy without developmental delay: further evidence for phenotypic variability.

Wallerstein R, Kacmar J, Anderson CE, Jackson L. Wallerstein R, et al. Am J Med Genet. 1997 Jan 20;68(2):216-8. Am J Med Genet. 1997. PMID: 9028461

2

Diagnosis of a complex chromosomal rearrangement using fluorescent in situ hybridisation.

Wallerstein R, Gibas L, Anderson CE, Jackson L. Wallerstein R, et al. J Med Genet. 1996 Sep;33(9):793-4. doi: 10.1136/jmg.33.9.793. J Med Genet. 1996. PMID: 8880585 Free PMC article.

3

Submicroscopic deletions at 16p13.3 in Rubinstein-Taybi syndrome: frequency and clinical manifestations in a North American population.

Wallerstein R, Anderson CE, Hay B, Gupta P, Gibas L, Ansari K, Cowchock FS, Weinblatt V, Reid C, Levitas A, Jackson L. Wallerstein R, et al. J Med Genet. 1997 Mar;34(3):203-6. doi: 10.1136/jmg.34.3.203. J Med Genet. 1997. PMID: 9132490 Free PMC article.

4

Ring chromosome 4 mosaicism coincidence of oligomeganephronia and signs of Seckel syndrome.

Anderson CE, Wallerstein R, Zamerowski ST, Witzleben C, Hoyer JR, Gibas L, Jackson LG. Anderson CE, et al. Among authors: wallerstein r. Am J Med Genet. 1997 Oct 31;72(3):281-5. Am J Med Genet. 1997. PMID: 9332654

5

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

6

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.

7

Extended survival in a new case of ter Haar syndrome: further delineation of the syndrome.

Wallerstein R, Scott CI Jr, Nicholson L. Wallerstein R, et al. Am J Med Genet. 1997 Jun 13;70(3):267-72. doi: 10.1002/(sici)1096-8628(19970613)70:3<267::aid-ajmg10>3.0.co;2-j. Am J Med Genet. 1997. PMID: 9188664

8

Novel ITGB4 mutations in lethal and nonlethal variants of epidermolysis bullosa with pyloric atresia: missense versus nonsense.

Pulkkinen L, Rouan F, Bruckner-Tuderman L, Wallerstein R, Garzon M, Brown T, Smith L, Carter W, Uitto J. Pulkkinen L, et al. Among authors: wallerstein r. Am J Hum Genet. 1998 Nov;63(5):1376-87. doi: 10.1086/302116. Am J Hum Genet. 1998. PMID: 9792864 Free PMC article.

9

Robinow syndrome with developmental brain dysplasia.

Guillén-Navarro E, Wallerstein R, Reich E, Zajac L, Ostrer H. Guillén-Navarro E, et al. Among authors: wallerstein r. Am J Med Genet. 1997 Nov 28;73(1):98-9. doi: 10.1002/(sici)1096-8628(19971128)73:1<98::aid-ajmg23>3.0.co;2-l. Am J Med Genet. 1997. PMID: 9375934 No abstract available.

10

A new case of Grange syndrome without cardiac findings.

Wallerstein R, Augustyn AM, Wallerstein D, Elton L, Tejeiro B, Johnson V, Lieberman K. Wallerstein R, et al. Among authors: wallerstein d. Am J Med Genet A. 2006 Jun 15;140(12):1316-20. doi: 10.1002/ajmg.a.31125. Am J Med Genet A. 2006. PMID: 16691574

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