Vekemans M - Search Results

1

Splotch (Sp2H), a mutation affecting development of the mouse neural tube, shows a deletion within the paired homeodomain of Pax-3.

Epstein DJ, Vekemans M, Gros P. Epstein DJ, et al. Among authors: vekemans m. Cell. 1991 Nov 15;67(4):767-74. doi: 10.1016/0092-8674(91)90071-6. Cell. 1991. PMID: 1682057

2

A chromosome marker for the early detection of mouse embryos carrying the neural tube defect mutation splotch.

Kapron-Brás CM, Vekemans MJ, Trasler DG. Kapron-Brás CM, et al. Among authors: vekemans mj. Can J Genet Cytol. 1986 Oct;28(5):862-6. doi: 10.1139/g86-120. Can J Genet Cytol. 1986. PMID: 3801972

3

An investigation of factors influencing the survival of trisomic fetuses in the mouse.

Vekemans M. Vekemans M. Prog Clin Biol Res. 1989;311:245-62. Prog Clin Biol Res. 1989. PMID: 2771998

4

Cytogenetic analysis of Wilms' tumor: evidence of a multistep process.

Vekemans M, De Braekeleer M, de Chadarevian JP. Vekemans M, et al. Oncology. 1989;46(5):306-9. doi: 10.1159/000226738. Oncology. 1989. PMID: 2550862

5

Translocation between chromosomes 6 and 15 (45,XX,t(6;15)(q25;q11.2)) with further evidence for lack of imprinting of the insulin-like growth factor II/mannose-6-phosphate receptor in humans.

Treacy E, Polychronakos C, Vekemans M, Eydoux P, Blaichman S, Scarpelli H, Ross M, Xu Y, Der Kaloustian VM. Treacy E, et al. Among authors: vekemans m. J Med Genet. 1996 Jan;33(1):42-6. doi: 10.1136/jmg.33.1.42. J Med Genet. 1996. PMID: 8825047 Free PMC article.

6

Genetic analysis of the maternal factors controlling the survival of trisomy 16 mouse fetuses.

Demczuk S, Vekemans M. Demczuk S, et al. Among authors: vekemans m. Teratology. 1993 Apr;47(4):311-9. doi: 10.1002/tera.1420470408. Teratology. 1993. PMID: 8322225

7

Characterization of a region-specific library of microclones in the vicinity of the Bcg and splotch loci on mouse chromosome 1.

Epstein DJ, Bardeesy N, Vidal S, Malo D, Weith A, Vekemans M, Gros P. Epstein DJ, et al. Among authors: vekemans m. Genomics. 1994 Jan 1;19(1):163-6. doi: 10.1006/geno.1994.1029. Genomics. 1994. PMID: 8188220

8

A presumptive translocation 1p;2q resulting in duplication 1p and deletion 2q.

Halal F, Vekemans M, Der Kaloustian VM. Halal F, et al. Among authors: vekemans m. Am J Med Genet. 1989 Mar;32(3):376-9. doi: 10.1002/ajmg.1320320322. Am J Med Genet. 1989. PMID: 2658588 Review.

9

Distal deletion of chromosome 1q in an adult.

Halal F, Vekemans M, Kaplan P, Zeesman S. Halal F, et al. Among authors: vekemans m. Am J Med Genet. 1990 Mar;35(3):379-82. doi: 10.1002/ajmg.1320350313. Am J Med Genet. 1990. PMID: 2137964

10

Molecular characterization of a deletion encompassing the splotch mutation on mouse chromosome 1.

Epstein DJ, Malo D, Vekemans M, Gros P. Epstein DJ, et al. Among authors: vekemans m. Genomics. 1991 May;10(1):89-93. doi: 10.1016/0888-7543(91)90488-z. Genomics. 1991. PMID: 2045114

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