Teshima I - Search Results

1

Velo-cardio-facial syndrome: Implications of microdeletion 22q11 for schizophrenia and mood disorders.

Arnold PD, Siegel-Bartelt J, Cytrynbaum C, Teshima I, Schachar R. Arnold PD, et al. Among authors: teshima i. Am J Med Genet. 2001 May 8;105(4):354-62. doi: 10.1002/ajmg.1359. Am J Med Genet. 2001. PMID: 11378850

2

FISH detection of chromosome 15 deletions in Prader-Willi and Angelman syndromes.

Teshima I, Chadwick D, Chitayat D, Kobayashi J, Ray P, Shuman C, Siegel-Bartelt J, Strasberg P, Weksberg R. Teshima I, et al. Am J Med Genet. 1996 Mar 29;62(3):217-23. doi: 10.1002/(sici)1096-8628(19960329)62:3<216::aid-ajmg3>3.3.co;2-0. Am J Med Genet. 1996. PMID: 8882776

3

Microdeletion 22q11.2: clinical data and deletion size.

Kerstjens-Frederikse WS, Kurahashi H, Driscoll DA, Budarf ML, Emanuel BS, Beatty B, Scheidl T, Siegel-Bartelt J, Henderson K, Cytrynbaum C, Nie G, Teshima I. Kerstjens-Frederikse WS, et al. Among authors: teshima i. J Med Genet. 1999 Sep;36(9):721-3. J Med Genet. 1999. PMID: 10507735 Free PMC article. No abstract available.

4

Patients with deletions of 9q22q34 do not define a syndrome: three case reports and a literature review.

Farrell SA, Siegel-Bartelt J, Teshima I. Farrell SA, et al. Among authors: teshima i. Clin Genet. 1991 Sep;40(3):207-14. doi: 10.1111/j.1399-0004.1991.tb03078.x. Clin Genet. 1991. PMID: 1773536 Review.

5

Deletion 4q21/4q22 syndrome: two patients with de novo 4q21.3q23 and 4q13.2q23 deletions.

Nowaczyk MJ, Teshima IE, Siegel-Bartelt J, Clarke JT. Nowaczyk MJ, et al. Among authors: teshima ie. Am J Med Genet. 1997 Apr 14;69(4):400-5. Am J Med Genet. 1997. PMID: 9098490

6

Craniosynostosis associated with partial duplication of 15q and deletion of 2q.

Van Allen MI, Siegel-Bartelt J, Feigenbaum A, Teshima IE. Van Allen MI, et al. Among authors: teshima ie. Am J Med Genet. 1992 Jul 1;43(4):688-92. doi: 10.1002/ajmg.1320430407. Am J Med Genet. 1992. PMID: 1621758

7

Holoprosencephaly and cleidocranial dysplasia in a patient due to two position-effect mutations: case report and review of the literature.

Fernandez BA, Siegel-Bartelt J, Herbrick JA, Teshima I, Scherer SW. Fernandez BA, et al. Among authors: teshima i. Clin Genet. 2005 Oct;68(4):349-59. doi: 10.1111/j.1399-0004.2005.00498.x. Clin Genet. 2005. PMID: 16143022 Review.

8

Malignant hematological disorders in children with Wolf-Hirschhorn syndrome.

Sharathkumar A, Kirby M, Freedman M, Abdelhaleem M, Chitayat D, Teshima IE, Dror Y. Sharathkumar A, et al. Am J Med Genet A. 2003 Jun 1;119A(2):194-9. doi: 10.1002/ajmg.a.20080. Am J Med Genet A. 2003. PMID: 12749063

9

Syndrome of proximal interstitial deletion 4p15: report of three cases and review of the literature.

Chitayat D, Ruvalcaba RH, Babul R, Teshima IE, Posnick JC, Vekemans MJ, Scarpelli H, Thuline H. Chitayat D, et al. Among authors: teshima ie. Am J Med Genet. 1995 Jan 16;55(2):147-54. doi: 10.1002/ajmg.1320550203. Am J Med Genet. 1995. PMID: 7717413 Review.

10

Partial tetrasomy with triplication of chromosome (5) (p14-p15.33) in a patient with severe multiple congenital anomalies.

Harrison KJ, Teshima IE, Silver MM, Jay V, Unger S, Robinson WP, James A, Levin A, Chitayat D. Harrison KJ, et al. Among authors: teshima ie. Am J Med Genet. 1998 Sep 1;79(2):103-7. Am J Med Genet. 1998. PMID: 9741467

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