Fox J - Search Results

1

A common breakpoint on 11q23 in carriers of the constitutional t(11;22) translocation.

Edelmann L, Spiteri E, McCain N, Goldberg R, Pandita RK, Duong S, Fox J, Blumenthal D, Lalani SR, Shaffer LG, Morrow BE. Edelmann L, et al. Among authors: fox j. Am J Hum Genet. 1999 Dec;65(6):1608-16. doi: 10.1086/302689. Am J Hum Genet. 1999. PMID: 10577914 Free PMC article.

2

Mosaicism with a normal cell line and an unbalanced structural rearrangement.

Zaslav AL, Fallet S, Blumenthal D, Jacob J, Fox J. Zaslav AL, et al. Among authors: fox j. Am J Med Genet. 1999 Jan 1;82(1):15-9. Am J Med Genet. 1999. PMID: 9916836 Review.

3

Prenatal diagnosis of a rare inherited heterochromatic variant chromosome 4.

Zaslav AL, Pierno G, Fougner A, Jacob J, Shikora G, Kazi R, Blumenthal D, Alexander F, Fox JE. Zaslav AL, et al. Among authors: fox je. Am J Med Genet A. 2004 May 1;126A(4):420-2. doi: 10.1002/ajmg.a.20594. Am J Med Genet A. 2004. PMID: 15098241

4

A rare inherited euchromatic heteromorphism on chromosome 1.

Zaslav AL, Blumenthal D, Fox JE, Thomson KA, Segraves R, Weinstein ME. Zaslav AL, et al. Among authors: fox je. Prenat Diagn. 1993 Jul;13(7):569-73. doi: 10.1002/pd.1970130706. Prenat Diagn. 1993. PMID: 8415421

5

Prenatal diagnosis of trisomy 4 mosaicism.

Zaslav AL, Blumenthal D, Willner JP, Pierno G, Jacob J, Fox JE. Zaslav AL, et al. Among authors: fox je. Am J Med Genet. 2000 Dec 11;95(4):381-4. Am J Med Genet. 2000. PMID: 11186894 Review.

6

Four sibs with arterial tortuosity: description and review of the literature.

Pletcher BA, Fox JE, Boxer RA, Singh S, Blumenthal D, Cohen T, Brunson S, Tafreshi P, Kahn E. Pletcher BA, et al. Among authors: fox je. Am J Med Genet. 1996 Dec 11;66(2):121-8. doi: 10.1002/(SICI)1096-8628(19961211)66:2<121::AID-AJMG1>3.0.CO;2-U. Am J Med Genet. 1996. PMID: 8958317 Review.

7

Infant with mos45,x/46,XY/47,XYY/48,XYYY: genetic and clinical findings.

Fox JE, Blumenthal D, Brock W, Kreitzer P, Cooper R, Anderson D, Pleak R, Ehrenfreund L, Freedman S, Zaslav AL. Fox JE, et al. Am J Med Genet. 1995 Dec 4;59(4):435-40. doi: 10.1002/ajmg.1320590408. Am J Med Genet. 1995. PMID: 8585562

8

Prenatal diagnosis of trisomy 3 mosaicism.

Zaslav AL, Pierno G, Davis J, Fougner A, Jacob J, Kazi R, Blumenthal D, Sturim S, Shaham M, Fox J. Zaslav AL, et al. Among authors: fox j. Prenat Diagn. 2004 Sep;24(9):693-6. doi: 10.1002/pd.963. Prenat Diagn. 2004. PMID: 15386452 Review.

9

Clinical features associated with copy number variations of the 14q32 imprinted gene cluster.

Rosenfeld JA, Fox JE, Descartes M, Brewer F, Stroud T, Gorski JL, Upton SJ, Moeschler JB, Monteleone B, Neill NJ, Lamb AN, Ballif BC, Shaffer LG, Ravnan JB. Rosenfeld JA, et al. Among authors: fox je. Am J Med Genet A. 2015 Feb;167A(2):345-53. doi: 10.1002/ajmg.a.36866. Am J Med Genet A. 2015. PMID: 25756153

10

Significance of a prenatally diagnosed del(10)(q23).

Zaslav AL, Fox JE, Jacob J, Kazi R, Allan S, Shklooskaya T, Sohal D, Kleyman SM, Verma RS. Zaslav AL, et al. Among authors: fox je. Am J Med Genet. 2002 Jan 15;107(2):174-6. doi: 10.1002/ajmg.10112. Am J Med Genet. 2002. PMID: 11807894

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