Overhauser J - Search Results

1

Ablepharon macrostomia syndrome with associated cutis laxa: possible localization to 18q.

Pellegrino JE, Schnur RE, Boghosian-Sell L, Strathdee G, Overhauser J, Spinner NB, Stump T, Grace K, Zackai EH. Pellegrino JE, et al. Among authors: overhauser j. Hum Genet. 1996 Apr;97(4):532-6. doi: 10.1007/BF02267081. Hum Genet. 1996. PMID: 8834257

2

Physical mapping of the holoprosencephaly critical region in 18p11.3.

Overhauser J, Mitchell HF, Zackai EH, Tick DB, Rojas K, Muenke M. Overhauser J, et al. Am J Hum Genet. 1995 Nov;57(5):1080-5. Am J Hum Genet. 1995. PMID: 7485158 Free PMC article.

3

Molecular mapping of the Edwards syndrome phenotype to two noncontiguous regions on chromosome 18.

Boghosian-Sell L, Mewar R, Harrison W, Shapiro RM, Zackai EH, Carey J, Davis-Keppen L, Hudgins L, Overhauser J. Boghosian-Sell L, et al. Among authors: overhauser j. Am J Hum Genet. 1994 Sep;55(3):476-83. Am J Hum Genet. 1994. PMID: 8079991 Free PMC article.

4

Interstitial deletions are not the main mechanism leading to 18q deletions.

Strathdee G, Harrison W, Riethman HC, Goodart SA, Overhauser J. Strathdee G, et al. Among authors: overhauser j. Am J Hum Genet. 1994 Jun;54(6):1085-91. Am J Hum Genet. 1994. PMID: 8198131 Free PMC article.

5

Molecular analysis of the 18q- syndrome--and correlation with phenotype.

Kline AD, White ME, Wapner R, Rojas K, Biesecker LG, Kamholz J, Zackai EH, Muenke M, Scott CI Jr, Overhauser J. Kline AD, et al. Among authors: overhauser j. Am J Hum Genet. 1993 May;52(5):895-906. Am J Hum Genet. 1993. PMID: 8488839 Free PMC article. Review.

6

Analysis of clinical variation seen in patients with 18q terminal deletions.

Strathdee G, Zackai EH, Shapiro R, Kamholz J, Overhauser J. Strathdee G, et al. Among authors: overhauser j. Am J Med Genet. 1995 Dec 4;59(4):476-83. doi: 10.1002/ajmg.1320590414. Am J Med Genet. 1995. PMID: 8585568

7

Neuropsychiatry of 18q- syndrome.

Mahr RN, Moberg PJ, Overhauser J, Strathdee G, Kamholz J, Loevner LA, Campbell H, Zackai EH, Reber ME, Mozley DP, Brown L, Turetsky BI, Shapiro RM. Mahr RN, et al. Among authors: overhauser j. Am J Med Genet. 1996 Apr 9;67(2):172-8. doi: 10.1002/(SICI)1096-8628(19960409)67:2<172::AID-AJMG7>3.0.CO;2-U. Am J Med Genet. 1996. PMID: 8723044

8

Tourette syndrome in a pedigree with a 7;18 translocation: identification of a YAC spanning the translocation breakpoint at 18q22.3.

Boghosian-Sell L, Comings DE, Overhauser J. Boghosian-Sell L, et al. Among authors: overhauser j. Am J Hum Genet. 1996 Nov;59(5):999-1005. Am J Hum Genet. 1996. PMID: 8900226 Free PMC article.

9

Molecular characterization of patients with 18q23 deletions.

Strathdee G, Sutherland R, Jonsson JJ, Sataloff R, Kohonen-Corish M, Grady D, Overhauser J. Strathdee G, et al. Among authors: overhauser j. Am J Hum Genet. 1997 Apr;60(4):860-8. Am J Hum Genet. 1997. PMID: 9106532 Free PMC article.

10

A new deletion of 18q23 with few typical features of the 18q- syndrome.

Kohonen-Corish M, Strathdee G, Overhauser J, McDonald T, Jammu V. Kohonen-Corish M, et al. Among authors: overhauser j. J Med Genet. 1996 Mar;33(3):240-3. doi: 10.1136/jmg.33.3.240. J Med Genet. 1996. PMID: 8728701 Free PMC article.

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