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Results:
1-12
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Results: 12
Authors:
Grange, G
Tantau, J
Pannier, E
Aubry, MC
Viot, G
Fallet-Bianco, C
Terrasse, G
Cabrol, D
Citation: G. Grange et al., Prenatal diagnosis of fetal tail and postabortum anatomical description, ULTRASOUN O, 18(5), 2001, pp. 531-533
Authors:
Campeotto, F
Naudin, C
Viot, G
Dupont, C
Citation: F. Campeotto et al., Rectal bleeding and rectal picking in Prader-Willi syndrome, ARCH PED, 8(10), 2001, pp. 1075-1077
Authors:
De Leersnyder, H
de Blois, MC
Claustrat, B
Romana, S
Albrecht, U
von Kleist-Retzow, JC
Delobel, B
Viot, G
Lyonnet, S
Vekemans, M
Munnich, A
Citation: H. De Leersnyder et al., Inversion of the circadian rhythm of melatonin in the Smith-Magenis syndrome, J PEDIAT, 139(1), 2001, pp. 111-116
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:
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
Radford, I
Viot, G
Edery, P
Munnich, A
Tardieu, M
Vekemans, M
Citation: L. Faivre et al., Cerebellar ataxia and mental retardation in a child with an inherited satellited chromosome 4q, ANN GENET, 43(1), 2000, pp. 35-38
Authors:
Dufourcq-Lagelouse, R
Lambert, N
Duval, M
Viot, G
Vilmer, E
Fischer, A
Prieur, M
de Saint Basile, G
Citation: R. Dufourcq-lagelouse et al., Chediak-Higashi syndrome associated with maternal uniparental isodisomy ofchromosome 1, EUR J HUM G, 7(6), 1999, pp. 633-637
Authors:
Cormier-Daire, V
Belin, V
Cusin, V
Viot, G
Girlich, D
Toutain, A
Moncla, A
Vekemans, M
Le Merrer, M
Munnich, A
Citation: V. Cormier-daire et al., SHOX gene mutations and deletions in dyschondrosteosis or Leri-Weill syndrome, ACT PAEDIAT, 88, 1999, pp. 55-59
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:
Favire, L
Morichon-Delvallez, N
Viot, G
Martinovic, J
Pinson, MP
Aubry, JP
Raclin, V
Edery, P
Dumez, Y
Munnich, A
Vekemans, M
Citation: L. Favire et al., Prenatal detection of a 1p36 deletion in a fetus with multiple malformations and a review of the literature, PRENAT DIAG, 19(1), 1999, pp. 49-53
Authors:
Manouvrier, S
Boute, O
Viot, G
Delobel, B
Citation: S. Manouvrier et al., Deletion of chromosome 4p detected by FISH in a girl with normal high resolution karyotype, CLIN GENET, 55(2), 1999, pp. 127-129
Authors:
Bonnet, D
Rustin, P
Rotig, A
de Lonlay, P
Viot, G
Munnich, A
Sidi, D
Citation: D. Bonnet et al., Metabolic and genetic investigations of cardiomyopathy in childhood., ARCH MAL C, 92(11), 1999, pp. 1509-1514
Risultati:
1-12
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