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Items: 8

1.

Identification of proximal 1p36 deletions using array-CGH: a possible new syndrome.

Kang SH, Scheffer A, Ou Z, Li J, Scaglia F, Belmont J, Lalani SR, Roeder E, Enciso V, Braddock S, Buchholz J, Vacha S, Chinault AC, Cheung SW, Bacino CA.

Clin Genet. 2007 Oct;72(4):329-38.

PMID:
17850629
2.

Connexin43 deficiency causes dysregulation of coronary vasculogenesis.

Walker DL, Vacha SJ, Kirby ML, Lo CW.

Dev Biol. 2005 Aug 15;284(2):479-98.

3.

Extensive sex-specific nonadditivity of gene expression in Drosophila melanogaster.

Gibson G, Riley-Berger R, Harshman L, Kopp A, Vacha S, Nuzhdin S, Wayne M.

Genetics. 2004 Aug;167(4):1791-9.

4.

PTEN mutations and proteus syndrome.

Biesecker LG, Rosenberg MJ, Vacha S, Turner JT, Cohen MM.

Lancet. 2001 Dec 15;358(9298):2079-80. No abstract available.

PMID:
11755638
5.

Sudden death caused by pulmonary thromboembolism in Proteus syndrome.

Slavotinek AM, Vacha SJ, Peters KF, Biesecker LG.

Clin Genet. 2000 Nov;58(5):386-9.

PMID:
11140839
6.

Discordance of oral-facial-digital syndrome type 1 in monozygotic twin girls.

Shotelersuk V, Tifft CJ, Vacha S, Peters KF, Biesecker LG.

Am J Med Genet. 1999 Sep 17;86(3):269-73.

PMID:
10482878
8.

Detection and separation of tricresyl phosphate by paper chromatography.

PATEL TB, BOMAN TJ, DASTUR NN, VACHA SM, SEN GUPTA G, TASKER K.

Indian J Med Sci. 1962 Feb;16:133-4. No abstract available.

PMID:
14484313

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