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Results:
1-17
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Results: 17
Authors:
Mahieu-Caputo, D
Sonigo, P
Amiel, J
Simon, I
Aubry, MC
Lemerrer, M
Delezoide, AL
Gigarel, N
Dommergues, M
Dumez, Y
Citation: D. Mahieu-caputo et al., Prenatal diagnosis of sporadic Apert syndrome: A sequential diagnostic approach combining three-dimensional computed tomography and molecular biology, FETAL DIAGN, 16(1), 2001, pp. 10-12
Authors:
Wysolmerski, JJ
Cormier, S
Philbrick, WM
Dann, P
Zhang, JP
Roume, J
Delezoide, AL
Silve, C
Citation: Jj. Wysolmerski et al., Absence of functional type 1 parathyroid hormone (PTH)/PTH-related proteinreceptors in humans is associated with abnormal breast development and tooth impaction, J CLIN END, 86(4), 2001, pp. 1788-1794
Authors:
Fougerousse, F
Anderson, LVB
Delezoide, AL
Suel, L
Durand, M
Beckmann, JS
Citation: F. Fougerousse et al., Calpain3 expression during human cardiogenesis, NEUROMUSC D, 10(4-5), 2000, pp. 251-256
Developmentally regulated expression of the murine ortholog of the potassium channel KIR4.2 (KCNJ15)
Authors:
Thiery, E
Gosset, P
Damotte, D
Delezoide, AL
de Saint-Sauveur, N
Vayssettes, C
Creau, N
Citation: E. Thiery et al., Developmentally regulated expression of the murine ortholog of the potassium channel KIR4.2 (KCNJ15), MECH DEVEL, 95(1-2), 2000, pp. 313-316
Authors:
Rachidi, M
Lopes, C
Gassanova, S
Sinet, PM
Vekemans, M
Attie, T
Delezoide, AL
Delabar, JM
Citation: M. Rachidi et al., Regional and cellular specificity of the expression of TPRD, the tetratricopeptide Down syndrome gene, during human embryonic development, MECH DEVEL, 93(1-2), 2000, pp. 189-193
Authors:
Guipponi, M
Brunschwig, K
Chamoun, Z
Scott, HS
Shibuya, K
Kudoh, J
Delezoide, AL
El Samadi, S
Chettouh, Z
Rossier, C
Shimizu, N
Mueller, F
Delabar, JM
Antonarakis, SE
Citation: M. Guipponi et al., C21orf5, a novel human chromosome 21 gene, has a Caenorhabditis elegans ortholog (pad-1) required for embryonic patterning, GENOMICS, 68(1), 2000, pp. 30-40
Authors:
Legeai-Mallet, L
Rossi, A
Benoist-Lasselin, C
Piazza, R
Malet, JF
Delezoide, AL
Munnich, A
Bonaventure, J
Zylberberg, L
Citation: L. Legeai-mallet et al., EXT 1 gene mutation induces chondrocyte cytoskeletal abnormalities and defective collagen expression in the exostoses, J BONE MIN, 15(8), 2000, pp. 1489-1500
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:
Tellier, AL
Amiel, J
Delezoide, AL
Audollent, S
Auge, J
Esnault, D
Encha-Razavi, F
Munnich, A
Lyonnet, S
Vekemans, M
Attie-Bitach, T
Citation: Al. Tellier et al., Expression of the PAX2 gene in human embryos and exclusion in the CHARGE syndrome, AM J MED G, 93(2), 2000, pp. 85-88
Authors:
Mahieu-Caputo, D
Dommergues, M
Delezoide, AL
Lacoste, M
Cai, Y
Narcy, F
Jolly, D
Gonzales, M
Dumez, Y
Gubler, MC
Citation: D. Mahieu-caputo et al., Twin-to-twin transfusion syndrome - Role of the fetal renin-angiotensin system, AM J PATH, 156(2), 2000, pp. 629-636
Authors:
Benachi, A
Delezoide, AL
Chailley-Heu, B
Preece, M
Bourbon, JR
Ryder, T
Citation: A. Benachi et al., Ultrastructural evaluation of lung maturation in a sheep model of diaphragmatic hernia and tracheal occlusion, AM J RESP C, 20(4), 1999, pp. 805-812
Authors:
Odent, S
Attie-Bitach, T
Blayau, M
Mathieu, M
Auge, J
Delezoide, AL
Le Gall, JY
Le Marec, B
Munnich, A
David, V
Vekemans, M
Citation: S. Odent et al., Expression of the Sonic hedgehog (SHH) gene during early human developmentand phenotypic expression of new mutations causing holoprosencephaly, HUM MOL GEN, 8(9), 1999, pp. 1683-1689
Authors:
Odent, S
Attie-Bitach, T
Blayau, M
Mathieu, M
Auge, J
Delezoide, AL
Le Gall, JY
Le Marec, B
Munnich, A
David, V
Vekemans, M
Citation: S. Odent et al., Expression of the Sonic hedgehog (SHH) gene during early human developmentand phenotypic expression of new mutations causing holoprosencephaly (vol 8, pg 1683, 1999), HUM MOL GEN, 8(12), 1999, pp. 2335-2335
Authors:
Lajeunie, E
Cameron, R
El Ghouzzi, V
de Parseval, N
Journeau, P
Gonzales, M
Delezoide, AL
Bonaventure, J
Le Merrer, M
Renier, D
Citation: E. Lajeunie et al., Clinical variability in patients with Apert's syndrome, J NEUROSURG, 90(3), 1999, pp. 443-447
Authors:
Odent, S
Loget, P
Le Marec, B
Delezoide, AL
Maroteaux, P
Citation: S. Odent et al., Unusual fan shaped ossification in a female fetus with radiological features of boomerang dysplasia, J MED GENET, 36(4), 1999, pp. 330-332
Authors:
Faivre, L
Delezoide, AL
Narcy, F
Razavi, F
Bouvier, R
Cormier-Daire, V
Briard, ML
Lyonnet, S
Vekemans, M
Munnich, A
Le Merrer, M
Citation: L. Faivre et al., A new lethal syndrome of exomphalos, short limbs, and macrogonadism, J MED GENET, 36(2), 1999, pp. 131-136
Authors:
Attie-Bitach, T
Abitbol, M
Gerard, M
Delezoide, AL
Auge, J
Pelet, A
Amiel, J
Pachnis, V
Munnich, A
Lyonnet, S
Vekemans, M
Citation: T. Attie-bitach et al., Expression of the RET proto-oncogene in human embryos, AM J MED G, 80(5), 1998, pp. 481-486
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