Results
|
1.
|
|
|
2.
|
|
|
3.
|
|
|
4.
|
|
|
5.
|
MLPA screening reveals novel subtelomeric rearrangements in holoprosencephaly. [electronic resource] by
- Bendavid, Claude
- Dubourg, Christèle
- Pasquier, Laurent
- Gicquel, Isabelle
- Le Gallou, Simon
- Mottier, Stéphanie
- Durou, Marie-Renée
- Henry, Catherine
- Odent, Sylvie
- David, Véronique
Producer: 20080128
In:
Human mutation vol. 28
Availability: No items available.
|
|
6.
|
Phenotypic variability of a 4q34-->qter inherited deletion: MRKH syndrome in the daughter, cardiac defect and Fallopian tube cancer in the mother. [electronic resource] by
- Bendavid, Claude
- Pasquier, Laurent
- Watrin, Tanguy
- Morcel, Karine
- Lucas, Josette
- Gicquel, Isabelle
- Dubourg, Christèle
- Henry, Catherine
- David, Véronique
- Odent, Sylvie
- Levêque, Jean
- Pellerin, Isabelle
- Guerrier, Daniel
Producer: 20070322
In:
European journal of medical genetics vol. 50
Availability: No items available.
|
|
7.
|
Molecular evaluation of foetuses with holoprosencephaly shows high incidence of microdeletions in the HPE genes. [electronic resource] by
- Bendavid, Claude
- Dubourg, Christèle
- Gicquel, Isabelle
- Pasquier, Laurent
- Saugier-Veber, Pascale
- Durou, Marie-Renée
- Jaillard, Sylvie
- Frébourg, Thierry
- Haddad, Bassem R
- Henry, Catherine
- Odent, Sylvie
- David, Véronique
Producer: 20070402
In:
Human genetics vol. 119
Availability: No items available.
|
|
8.
|
NOTCH, a new signaling pathway implicated in holoprosencephaly. [electronic resource] by
- Dupé, Valérie
- Rochard, Lucie
- Mercier, Sandra
- Le Pétillon, Yann
- Gicquel, Isabelle
- Bendavid, Claude
- Bourrouillou, Georges
- Kini, Usha
- Thauvin-Robinet, Christel
- Bohan, Timothy P
- Odent, Sylvie
- Dubourg, Christèle
- David, Véronique
Producer: 20110620
In:
Human molecular genetics vol. 20
Availability: No items available.
|
|
9.
|
Transcriptome variations in human CaCo-2 cells: a model for enterocyte differentiation and its link to iron absorption. [electronic resource] by
- Bédrine-Ferran, Hélène
- Le Meur, Nolwenn
- Gicquel, Isabelle
- Le Cunff, Martine
- Soriano, Nicolas
- Guisle, Isabelle
- Mottier, Stéphanie
- Monnier, Annabelle
- Teusan, Raluca
- Fergelot, Patricia
- Le Gall, Jean-Yves
- Léger, Jean
- Mosser, Jean
Producer: 20041026
In:
Genomics vol. 83
Availability: No items available.
|
|
10.
|
Array-CGH analysis indicates a high prevalence of genomic rearrangements in holoprosencephaly: an updated map of candidate loci. [electronic resource] by
- Bendavid, Claude
- Rochard, Lucie
- Dubourg, Christèle
- Seguin, Jonathan
- Gicquel, Isabelle
- Pasquier, Laurent
- Vigneron, Jaqueline
- Laquerrière, Annie
- Marcorelles, Pascale
- Jeanne-Pasquier, Corinne
- Rouleau, Caroline
- Jaillard, Sylvie
- Mosser, Jean
- Odent, Sylvie
- David, Veronique
Producer: 20091022
In:
Human mutation vol. 30
Availability: No items available.
|
|
11.
|
New findings for phenotype-genotype correlations in a large European series of holoprosencephaly cases. [electronic resource] by
- Mercier, Sandra
- Dubourg, Christèle
- Garcelon, Nicolas
- Campillo-Gimenez, Boris
- Gicquel, Isabelle
- Belleguic, Marion
- Ratié, Leslie
- Pasquier, Laurent
- Loget, Philippe
- Bendavid, Claude
- Jaillard, Sylvie
- Rochard, Lucie
- Quélin, Chloé
- Dupé, Valérie
- David, Véronique
- Odent, Sylvie
Producer: 20120210
In:
Journal of medical genetics vol. 48
Availability: No items available.
|