Siegel-Bartelt J - Search Results

1

Ocular manifestations of frontonasal dysplasia.

Roarty JD, Pron GE, Siegel-Bartelt J, Posnick JC, Buncic JR. Roarty JD, et al. Plast Reconstr Surg. 1994 Jan;93(1):25-30. doi: 10.1097/00006534-199401000-00004. Plast Reconstr Surg. 1994. PMID: 8278482

2

Cerebellar infarction in a patient with Waardenburg syndrome.

Narod SA, Siegel-Bartelt J, Hoffman HJ. Narod SA, et al. Am J Med Genet. 1988 Dec;31(4):903-7. doi: 10.1002/ajmg.1320310424. Am J Med Genet. 1988. PMID: 3239580

3

Infantile lethal variant of Simpson-Golabi-Behmel syndrome associated with hydrops fetalis.

Terespolsky D, Farrell SA, Siegel-Bartelt J, Weksberg R. Terespolsky D, et al. Am J Med Genet. 1995 Nov 20;59(3):329-33. doi: 10.1002/ajmg.1320590310. Am J Med Genet. 1995. PMID: 8599356

4

FGFR2 mutation associated with clinical manifestations consistent with Antley-Bixler syndrome.

Chun K, Siegel-Bartelt J, Chitayat D, Phillips J, Ray PN. Chun K, et al. Among authors: siegel bartelt j. Am J Med Genet. 1998 May 18;77(3):219-24. doi: 10.1002/(sici)1096-8628(19980518)77:3<219::aid-ajmg6>3.0.co;2-k. Am J Med Genet. 1998. PMID: 9605588

5

MRI findings in macrocephaly-cutis marmorata telangiectatica congenita.

Carcao M, Blaser SI, Grant RM, Weksberg R, Siegel-Bartelt J. Carcao M, et al. Among authors: siegel bartelt j. Am J Med Genet. 1998 Mar 5;76(2):165-7. Am J Med Genet. 1998. PMID: 9511980

6

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. Am J Med Genet. 1997 Apr 14;69(4):400-5. Am J Med Genet. 1997. PMID: 9098490

7

Hirschsprung disease, postaxial polydactyly, and atrial septal defect.

Nowaczyk MJ, James AG, Superina R, Siegel-Bartelt J. Nowaczyk MJ, et al. Am J Med Genet. 1997 Jan 10;68(1):74-5. doi: 10.1002/(sici)1096-8628(19970110)68:1<74::aid-ajmg14>3.0.co;2-l. Am J Med Genet. 1997. PMID: 8986280

8

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. Clin Genet. 1991 Sep;40(3):207-14. doi: 10.1111/j.1399-0004.1991.tb03078.x. Clin Genet. 1991. PMID: 1773536 Review.

9

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: siegel bartelt j. Am J Med Genet. 2001 May 8;105(4):354-62. doi: 10.1002/ajmg.1359. Am J Med Genet. 2001. PMID: 11378850

10

Additional EFNB1 mutations in craniofrontonasal syndrome.

Wallis D, Lacbawan F, Jain M, Der Kaloustian VM, Steiner CE, Moeschler JB, Losken HW, Kaitila II, Cantrell S, Proud VK, Carey JC, Day DW, Lev D, Teebi AS, Robinson LK, Hoyme HE, Al-Torki N, Siegel-Bartelt J, Mulliken JB, Robin NH, Saavedra D, Zackai EH, Muenke M. Wallis D, et al. Among authors: siegel bartelt j. Am J Med Genet A. 2008 Aug 1;146A(15):2008-12. doi: 10.1002/ajmg.a.32388. Am J Med Genet A. 2008. PMID: 18627045 Free PMC article. No abstract available.

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