Cytogenetics of mammalian embryonic development

gan Vekemans, M.
Cyhoeddwyd 1989

Influence of age on serum prolactin levels in women and men.

gan Vekemans, M, Robyn, C
Cyhoeddwyd 1975

Triploidy arising from a first meiotic non-disjunction in a mother carrying a reciprocal translocation.

gan Rochon, L, Vekemans, M J
Cyhoeddwyd 1990

Confined placental mosaicism.

gan Kalousek, D K, Vekemans, M
Cyhoeddwyd 1996

Holoprosencephaly and sacral agenesis in a fetus with a terminal deletion 7q36-->7qter.

gan Morichon-Delvallez, N, Delezoide, A L, Vekemans, M
Cyhoeddwyd 1993

Chromosomal breakage in normal and fragile X subjects using low folate culture conditions.

gan Vekemans, M, Popovich, B, Rosenblatt, D, Monroe, P
Cyhoeddwyd 1983

Circadian Periodicity of Serum Prolactin Concentration in Man

gan Nokin, J., Vekemans, M., L'Hermite, M., Robyn, C.
Cyhoeddwyd 1972

Intracellular folate distribution in cultured fibroblasts from patients with the fragile X syndrome.

gan Popovich, B W, Rosenblatt, D S, Cooper, B A, Vekemans, M
Cyhoeddwyd 1983

A contribution to the differential diagnosis of the "group of schizophrenias": structural abnormality of chromosome 4.

gan Palmour, R M, Miller, S, Fielding, A, Vekemans, M, Ervin, F R
Cyhoeddwyd 1994

Prolactin studies in normal subjects.

gan L'Hermite, M, Vekemans, M, Delvoye, P, Nokin, J, Robyn, C
Cyhoeddwyd 1973

Interstitial duplication of the short arm of chromosome 2: report of a new case and review.

gan Mégarbané, A, Souraty, N, Prieur, M, Theophile, D, Chédid, P, Augé, J, Vekemans, M
Cyhoeddwyd 1997

Folic acid blinded trial in identical twins with fragile X syndrome.

gan Rosenblatt, D S, Duschenes, E A, Hellstrom, F V, Golick, M S, Vekemans, M J, Zeesman, S F, Andermann, E
Cyhoeddwyd 1985

β(1)-adrenergic antagonists improve sleep and behavioural disturbances in a circadian disorder, Smith-Magenis syndrome

gan De Leersnyder, H., de Blois, M.-C., Vekemans, M., Sidi, D., Villain, E., Kindermans, C., Munnich, A.
Cyhoeddwyd 2001

Recurrent Williams-Beuren syndrome in a sibship suggestive of maternal germ-line mosaicism.

gan Kara-Mostefa, A, Raoul, O, Lyonnet, S, Amiel, J, Munnich, A, Vekemans, M, Magnier, S, Ossareh, B, Bonnefont, J P
Cyhoeddwyd 1999

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...

gan Treacy, E, Polychronakos, C, Vekemans, M, Eydoux, P, Blaichman, S, Scarpelli, H, Ross, M, Xu, Y, Der Kaloustian, V M
Cyhoeddwyd 1996

Cryptic terminal deletion of chromosome 9q34: a novel cause of syndromic obesity in childhood?

gan Cormier-Daire, V, Molinari, F, Rio, M, Raoul, O, de Blois, M-C, Romana, S, Vekemans, M, Munnich, A, Colleaux, L
Cyhoeddwyd 2003

Maternal uniparental heterodisomy of chromosome 14: chromosomal mechanism and clinical follow up

gan Sanlaville, D, Aubry, M, Dumez, Y, Nolen, M, Amiel, J, Pinson, M, Lyonnet, S, Munnich, A, Vekemans, M, Morichon-Delvalle..., N
Cyhoeddwyd 2000

NIPBL mutations and genetic heterogeneity in Cornelia de Lange syndrome

gan Borck, G, Redon, R, Sanlaville, D, Rio, M, Prieur, M, Lyonnet, S, Vekemans, M, Carter, N, Munnich, A, Colleaux, L, Cormier-Daire, V
Cyhoeddwyd 2004

A new lethal syndrome of exomphalos, short limbs, and macrogonadism

gan Faivre, L., Delezoide, A., Narcy, F., Razavi, F., Bouvier, R., Cormier-Daire, V., Briard, M., Lyonnet, S., Vekemans, M., Munnich, A., Le Merrer, M.
Cyhoeddwyd 1999

Pure partial 7p trisomy including the TWIST, HOXA, and GLI3 genes

gan MEGARBANE, A, LE LORC'H, M, ELGHEZAL, H, JOLY, G, GOSSET, P, SOURATY, N, SAMARAS, L, PRIEUR, M, VEKEMANS, M, TURLEAU, C, ROMANA, S
Cyhoeddwyd 2001