Overhauser J - Search Results

1

Clinical and molecular characterisation of 80 patients with 5p deletion: genotype-phenotype correlation.

Mainardi PC, Perfumo C, Calì A, Coucourde G, Pastore G, Cavani S, Zara F, Overhauser J, Pierluigi M, Bricarelli FD. Mainardi PC, et al. Among authors: overhauser j. J Med Genet. 2001 Mar;38(3):151-8. doi: 10.1136/jmg.38.3.151. J Med Genet. 2001. PMID: 11238681 Free PMC article.

2

The first three mosaic cri du chat syndrome patients with two rearranged cell lines.

Perfumo C, Cerruti Mainardi P, Calí A, Coucourde G, Zara F, Cavani S, Overhauser J, Bricarelli FD, Pierluigi M. Perfumo C, et al. Among authors: overhauser j. J Med Genet. 2000 Dec;37(12):967-72. doi: 10.1136/jmg.37.12.967. J Med Genet. 2000. PMID: 11186943 Free PMC article. No abstract available.

3

Growth charts for cri-du-chat syndrome: an international collaborative study.

Marinescu RC, Mainardi PC, Collins MR, Kouahou M, Coucourde G, Pastore G, Eaton-Evans J, Overhauser J. Marinescu RC, et al. Among authors: overhauser j. Am J Med Genet. 2000 Sep 11;94(2):153-62. doi: 10.1002/1096-8628(20000911)94:2<153::aid-ajmg8>3.0.co;2-#. Am J Med Genet. 2000. PMID: 10982972

4

Variability in a family with an insertion involving 5p.

Marinescu RC, Mamunes P, Kline AD, Schmidt J, Rojas K, Overhauser J. Marinescu RC, et al. Among authors: overhauser j. Am J Med Genet. 1999 Sep 17;86(3):258-63. Am J Med Genet. 1999. PMID: 10482876

5

Clinical phenotype and molecular analysis of a three-generation family with an interstitial deletion of the short arm of chromosome 5.

Keppen LD, Gollin SM, Edwards D, Sawyer J, Wilson W, Overhauser J. Keppen LD, et al. Among authors: overhauser j. Am J Med Genet. 1992 Oct 1;44(3):356-60. doi: 10.1002/ajmg.1320440317. Am J Med Genet. 1992. PMID: 1488985

6

No relationship between the size of the deletion and the level of developmental delay in cri-du-chat syndrome.

Marinescu RC, Johnson EI, Dykens EM, Hodapp RM, Overhauser J. Marinescu RC, et al. Among authors: overhauser j. Am J Med Genet. 1999 Sep 3;86(1):66-70. doi: 10.1002/(sici)1096-8628(19990903)86:1<66::aid-ajmg13>3.0.co;2-n. Am J Med Genet. 1999. PMID: 10440832

7

Characterization of a complex chromosomal rearrangement in a patient with a typical catlike cry and no other clinical findings of cri-du-chat syndrome.

Sreekantaiah C, Kronn D, Marinescu RC, Goldin B, Overhauser J. Sreekantaiah C, et al. Among authors: overhauser j. Am J Med Genet. 1999 Sep 17;86(3):264-8. Am J Med Genet. 1999. PMID: 10482877

8

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

9

Molecular cytogenetic determination of a deletion/duplication of 1q that results in a trisomy 18 syndrome-like phenotype.

Mewar R, Harrison W, Weaver DD, Palmer C, Davee MA, Overhauser J. Mewar R, et al. Among authors: overhauser j. Am J Med Genet. 1994 Aug 15;52(2):178-83. doi: 10.1002/ajmg.1320520211. Am J Med Genet. 1994. PMID: 7802005

10

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.

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