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Archives Des Maladies Du Coeur Et Des Vaisseaux
|
June 20, 2000
[Clinical spectrum of prenatal tetralogy of Fallot]
A Azancot, P Eydoux, E Vuillard, et al.
Journal of Medical Genetics
|
August 27, 1998
Association of the FcepsilonRIbeta gene with bronchial hyper-responsiveness in an Italian population
E Trabetti, V Cusin, G Malerba, et al.
Journal of Medical Genetics
|
January 14, 2000
Exclusion of chromosome 9 helps to identify mild variants of acromesomelic dysplasia Maroteaux type
L Faivre, M Le Merrer, A Megarbane, et al.
Acta Paediatrica (Oslo, Norway : 1992). Supplement
|
January 8, 2000
SHOX gene mutations and deletions in dyschondrosteosis or Leri-Weill syndrome
V Cormier-Daire, V Belin, V Cusin, et al.
Nature Genetics
|
May 20, 1998
SHOX mutations in dyschondrosteosis (Leri-Weill syndrome)
V Belin, V Cusin, G Viot, et al.
American Journal of Medical Genetics. Part A
|
August 2, 2005
Microcephaly is not mandatory for the diagnosis of mosaic variegated aneuploidy syndrome
P Callier, L Faivre, V Cusin, et al.
American Journal of Respiratory and Critical Care Medicine
|
October 13, 2000
Linkage analysis of chromosome 12 markers in Italian families with atopic asthmatic children
G Malerba, M C Lauciello, T Scherpbier, et al.
Journal of Medical Genetics
|
January 7, 2006
Clinical, molecular, and genotype-phenotype correlation studies from 25 cases of oral-facial-digital syndrome type 1: a French and Belgian collaborative study
C Thauvin-Robinet, M Cossée, V Cormier-Daire, et al.
Prenatal Diagnosis
|
November 14, 2012
What do French patients and geneticists think about prenatal and preimplantation diagnoses in Marfan syndrome?
F Coron, T Rousseau, G Jondeau, et al.
Clinical Genetics
|
March 20, 2013
Systematic molecular and cytogenetic screening of 100 patients with marfanoid syndromes and intellectual disability
P Callier, B Aral, N Hanna, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 10) with videos related to
Sort By:
Page
of 1
Archives Des Maladies Du Coeur Et Des Vaisseaux
|
June 20, 2000
[Clinical spectrum of prenatal tetralogy of Fallot]
A Azancot, P Eydoux, E Vuillard, et al.
Journal of Medical Genetics
|
August 27, 1998
Association of the FcepsilonRIbeta gene with bronchial hyper-responsiveness in an Italian population
E Trabetti, V Cusin, G Malerba, et al.
Journal of Medical Genetics
|
January 14, 2000
Exclusion of chromosome 9 helps to identify mild variants of acromesomelic dysplasia Maroteaux type
L Faivre, M Le Merrer, A Megarbane, et al.
Acta Paediatrica (Oslo, Norway : 1992). Supplement
|
January 8, 2000
SHOX gene mutations and deletions in dyschondrosteosis or Leri-Weill syndrome
V Cormier-Daire, V Belin, V Cusin, et al.
Nature Genetics
|
May 20, 1998
SHOX mutations in dyschondrosteosis (Leri-Weill syndrome)
V Belin, V Cusin, G Viot, et al.
American Journal of Medical Genetics. Part A
|
August 2, 2005
Microcephaly is not mandatory for the diagnosis of mosaic variegated aneuploidy syndrome
P Callier, L Faivre, V Cusin, et al.
American Journal of Respiratory and Critical Care Medicine
|
October 13, 2000
Linkage analysis of chromosome 12 markers in Italian families with atopic asthmatic children
G Malerba, M C Lauciello, T Scherpbier, et al.
Journal of Medical Genetics
|
January 7, 2006
Clinical, molecular, and genotype-phenotype correlation studies from 25 cases of oral-facial-digital syndrome type 1: a French and Belgian collaborative study
C Thauvin-Robinet, M Cossée, V Cormier-Daire, et al.
Prenatal Diagnosis
|
November 14, 2012
What do French patients and geneticists think about prenatal and preimplantation diagnoses in Marfan syndrome?
F Coron, T Rousseau, G Jondeau, et al.
Clinical Genetics
|
March 20, 2013
Systematic molecular and cytogenetic screening of 100 patients with marfanoid syndromes and intellectual disability
P Callier, B Aral, N Hanna, et al.
Page
of 1