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Developmental Biology
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December 3, 2016
Distinct requirements of wls, wnt9a, wnt5b and gpc4 in regulating chondrocyte maturation and timing of endochondral ossification
Irving Tc Ling, Lucie Rochard, Eric C Liao
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
January 28, 2010
Holoprosencephaly: An update on cytogenetic abnormalities
Claude Bendavid, Valérie Dupé, Lucie Rochard, et al.
Developmental Biology
|
June 29, 2013
Requirement for frzb and fzd7a in cranial neural crest convergence and extension mechanisms during zebrafish palate and jaw morphogenesis
George Kamel, Tatiana Hoyos, Lucie Rochard, et al.
Development (Cambridge, England)
|
June 12, 2016
Roles of Wnt pathway genes wls, wnt9a, wnt5b, frzb and gpc4 in regulating convergent-extension during zebrafish palate morphogenesis
Lucie Rochard, Stefanie D Monica, Irving T C Ling, et al.
Orphanet Journal of Rare Diseases
|
March 17, 2011
Utero-vaginal aplasia (Mayer-Rokitansky-Küster-Hauser syndrome) associated with deletions in known DiGeorge or DiGeorge-like loci
Karine Morcel, Tanguy Watrin, Laurent Pasquier, et al.
Human Molecular Genetics
|
January 4, 2011
NOTCH, a new signaling pathway implicated in holoprosencephaly
Valérie Dupé, Lucie Rochard, Sandra Mercier, et al.
Human Mutation
|
May 12, 2009
Array-CGH analysis indicates a high prevalence of genomic rearrangements in holoprosencephaly: an updated map of candidate loci
Claude Bendavid, Lucie Rochard, Christèle Dubourg, et al.
Journal of Medical Genetics
|
September 24, 2011
New findings for phenotype-genotype correlations in a large European series of holoprosencephaly cases
Sandra Mercier, Christèle Dubourg, Nicolas Garcelon, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 8) with videos related to
Sort By:
Page
of 1
Developmental Biology
|
December 3, 2016
Distinct requirements of wls, wnt9a, wnt5b and gpc4 in regulating chondrocyte maturation and timing of endochondral ossification
Irving Tc Ling, Lucie Rochard, Eric C Liao
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
January 28, 2010
Holoprosencephaly: An update on cytogenetic abnormalities
Claude Bendavid, Valérie Dupé, Lucie Rochard, et al.
Developmental Biology
|
June 29, 2013
Requirement for frzb and fzd7a in cranial neural crest convergence and extension mechanisms during zebrafish palate and jaw morphogenesis
George Kamel, Tatiana Hoyos, Lucie Rochard, et al.
Development (Cambridge, England)
|
June 12, 2016
Roles of Wnt pathway genes wls, wnt9a, wnt5b, frzb and gpc4 in regulating convergent-extension during zebrafish palate morphogenesis
Lucie Rochard, Stefanie D Monica, Irving T C Ling, et al.
Orphanet Journal of Rare Diseases
|
March 17, 2011
Utero-vaginal aplasia (Mayer-Rokitansky-Küster-Hauser syndrome) associated with deletions in known DiGeorge or DiGeorge-like loci
Karine Morcel, Tanguy Watrin, Laurent Pasquier, et al.
Human Molecular Genetics
|
January 4, 2011
NOTCH, a new signaling pathway implicated in holoprosencephaly
Valérie Dupé, Lucie Rochard, Sandra Mercier, et al.
Human Mutation
|
May 12, 2009
Array-CGH analysis indicates a high prevalence of genomic rearrangements in holoprosencephaly: an updated map of candidate loci
Claude Bendavid, Lucie Rochard, Christèle Dubourg, et al.
Journal of Medical Genetics
|
September 24, 2011
New findings for phenotype-genotype correlations in a large European series of holoprosencephaly cases
Sandra Mercier, Christèle Dubourg, Nicolas Garcelon, et al.
Page
of 1