Vekemans MJ - Search Results

1

Syndrome of proximal interstitial deletion 4p15: report of three cases and review of the literature.

Chitayat D, Ruvalcaba RH, Babul R, Teshima IE, Posnick JC, Vekemans MJ, Scarpelli H, Thuline H. Chitayat D, et al. Among authors: vekemans mj. Am J Med Genet. 1995 Jan 16;55(2):147-54. doi: 10.1002/ajmg.1320550203. Am J Med Genet. 1995. PMID: 7717413 Review.

2

Phocomelia, oligodactyly, and acrania: the Schinzel-Phocomelia syndrome.

Chitayat D, Stalker HJ, Vekemans M, Delneste D, Azouz EM. Chitayat D, et al. Am J Med Genet. 1993 Feb 1;45(3):297-9. doi: 10.1002/ajmg.1320450304. Am J Med Genet. 1993. PMID: 8123061

3

Duplication of 9q12-q33: a case report and implications for the dup(9q) syndrome.

Stalker HJ, Aymé S, Delneste D, Scarpelli H, Vekemans M, Der Kaloustian VM. Stalker HJ, et al. Am J Med Genet. 1993 Feb 15;45(4):456-9. doi: 10.1002/ajmg.1320450412. Am J Med Genet. 1993. PMID: 8465850 Review.

4

Trisomy 22 and facioauriculovertebral (Goldenhar) sequence.

Kobrynski L, Chitayat D, Zahed L, McGregor D, Rochon L, Brownstein S, Vekemans M, Albert DL. Kobrynski L, et al. Am J Med Genet. 1993 Apr 1;46(1):68-71. doi: 10.1002/ajmg.1320460111. Am J Med Genet. 1993. PMID: 8494034 Review.

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. 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

Interstitial tandem direct duplication of the long arm of chromosome 4 (q23-q27) and possible assignment of the structural gene encoding human aspartylglucosaminidase to this segment.

Halal F, Vekemans M, Chitayat D. Halal F, et al. Am J Med Genet. 1991 Jun 15;39(4):418-21. doi: 10.1002/ajmg.1320390412. Am J Med Genet. 1991. PMID: 1877620

7

Ring chromosome 20 and possible assignment of the structural gene encoding human carboxypeptidase-L to the distal segment of the long arm of chromosome 20.

Halal F, Chitayat D, Parikh H, Rosenblatt B, Tranchemontagne J, Vekemans M, Potier M. Halal F, et al. Am J Med Genet. 1992 Jun 1;43(3):576-9. doi: 10.1002/ajmg.1320430314. Am J Med Genet. 1992. PMID: 1605251

8

Distal deletion of chromosome 1q in an adult.

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

9

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

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

10

Canadian multicenter randomized clinical trial of chorion villus sampling and amniocentesis. chromosome mosaicism in CVS and amniocentesis samples.

Teshima IE, Kalousek DK, Vekemans MJ, Markovic V, Cox DM, Dallaire L, Gagne R, Lin JC, Ray M, Sergovich FR, et al. Teshima IE, et al. Among authors: vekemans mj. Prenat Diagn. 1992 May;12(5):443-66. doi: 10.1002/pd.1970120514. Prenat Diagn. 1992. PMID: 1523211 Clinical Trial.

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