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Results:
1-12
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Results: 12
Authors:
Colleaux, L
Rio, M
Heuertz, S
Moindrault, S
Turleau, C
Ozilou, C
Gosset, P
Raoult, O
Lyonnet, S
Cormier-Daire, V
Amiel, J
Le Merrer, M
Picq, M
de Blois, MC
Prieur, M
Romana, S
Cornelis, F
Vekemans, M
Munnich, A
Citation: L. Colleaux et al., A novel automated strategy for screening cryptic telomeric rearrangements in children with idiopathic mental retardation, EUR J HUM G, 9(5), 2001, pp. 319-327
Authors:
Rio, M
Ozilou, C
Cormier-Daire, V
Turleau, C
Prieur, M
Vekemans, M
Chauveau, P
Munnich, A
Colleaux, L
Citation: M. Rio et al., Partial maternal heterodisomy of chromosome 17q25 in a case of severe mental retardation, HUM GENET, 108(6), 2001, pp. 511-515
Authors:
Gekas, J
Thepot, F
Turleau, C
Siffroi, JP
Dadoune, JP
Wasels, R
Benzacken, B
Citation: J. Gekas et al., Chromosomal factors of infertility in candidate couples for ICSI: an equalrisk of constitutional aberrations in women and men, HUM REPR, 16(1), 2001, pp. 82-90
Authors:
Megarbane, A
Le Lorch, M
Elghezal, H
Joly, G
Gosset, P
Souraty, N
Samaras, L
Prieur, M
Vekemans, M
Turleau, C
Romana, SP
Citation: A. Megarbane et al., Pure partial 7p trisomy including the TWIST, HOXA, and GLI3 genes, J MED GENET, 38(3), 2001, pp. 178-182
Authors:
Joly, G
Lapierre, JM
Ozilou, C
Gosset, P
Aurias, A
de Blois, MC
Prieur, M
Raoul, O
Colleaux, L
Munnich, A
Romana, SP
Vekemans, M
Turleau, C
Citation: G. Joly et al., Comparative genomic hybridisation in mentally retarded patients with dysmorphic features and a normal karyotype, CLIN GENET, 60(3), 2001, pp. 212-219
Authors:
Fert-Ferrer, S
Guichet, A
Tantau, J
Delezoide, AL
Ozilou, C
Romana, SP
Gosset, P
Viot, G
Loison, S
Moraine, C
Morichon-Delvallez, N
Turleau, C
Vekemans, M
Prieur, M
Citation: S. Fert-ferrer et al., Subtle familial unbalanced translocation t(8;11)(p23.2;p15.5) in two fetuses with Beckwith-Wiedemann features, PRENAT DIAG, 20(6), 2000, pp. 511-515
Authors:
Megarbane, A
Gosset, P
Souraty, N
Lapierre, JM
Turleau, C
Vekemans, M
Loiselet, J
Prieur, M
Citation: A. Megarbane et al., Chromosome 7q22-q31 duplication: Report of a new case and review, AM J MED G, 95(2), 2000, pp. 164-168
Authors:
Faivre, L
Viot, G
Prieur, M
Turleau, C
Gosset, P
Romana, S
Munnich, A
Vekemans, M
Cormier-Daire, V
Citation: L. Faivre et al., Apparent Sotos syndrome (cerebral gigantism) in a child with trisomy 20p11.2-p12.1 mosaicism, AM J MED G, 91(4), 2000, pp. 273-276
Authors:
Faivre, L
Morichon-Delvallez, N
Viot, G
Larget-Piet, A
Narcy, F
Turleau, C
Pinson, MP
Dumez, Y
Munnich, A
Vekemans, M
Citation: L. Faivre et al., Prenatal diagnosis of a satellited non-acrocentric chromosome derived froma maternal translocation (10;13)(p13;p12) and review of literature, PRENAT DIAG, 19(3), 1999, pp. 282-286
Authors:
Briault, S
Odent, S
Lucas, J
Le Merrer, M
Turleau, C
Munnich, A
Moraine, C
Citation: S. Briault et al., Paracentric inversion of the X chromosome [inv(X)(q12q28)] in familial FG syndrome, AM J MED G, 86(2), 1999, pp. 112-114
Authors:
Sanlaville, D
Baumann, C
Lapierre, JM
Romana, S
Collot, N
Cacheux, V
Turleau, C
Tachdjian, G
Citation: D. Sanlaville et al., De novo inverted duplication 9p21pter involving telomeric repeated sequences, AM J MED G, 83(2), 1999, pp. 125-131
Authors:
Baud, O
Cormier-Daire, V
Lyonnet, S
Desjardins, L
Turleau, C
Doz, F
Citation: O. Baud et al., Dysmorphic phenotype and neurological impairment in 22 retinoblastoma patients with constitutional cytogenetic 13q deletion, CLIN GENET, 55(6), 1999, pp. 478-482
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