Search research articles
Contact Us
Filters
Showing results (31-40 of 110) with videos related to
Page
of 11
Sort By:
Pediatrie
|
January 1, 1993
[Value and limits of autopsy in perinatal medicine. A plea for complete perimortem evaluation]
P Bétrémieux, P Pladys, P Poulain, et al.
Annales De Biologie Clinique
|
January 9, 2004
[Genetic study of holoprosencephaly]
C Dubourg, L Lazaro, M Blayau, et al.
Annales D'Endocrinologie
|
February 15, 2002
[Pseudohypoparathyroidism or hypoparathyroidism? A misleading clinical presentation]
C Derrien, S Odent, C Henry, et al.
American Journal of Medical Genetics
|
August 17, 1999
Paracentric inversion of the X chromosome [inv(X)(q12q28)] in familial FG syndrome
S Briault, S Odent, J Lucas, et al.
Pediatrie
|
January 1, 1993
[Diffuse subcortical heterotopias of the gray matter]
C Treguier, P Muh, C Le Berre, et al.
Journal of Assisted Reproduction and Genetics
|
November 13, 2014
Gene dosage effects in 46, XY DSD: usefulness of CGH technologies for diagnosis
S Jaillard, A Bashamboo, L Pasquier, et al.
American Journal of Medical Genetics
|
October 23, 1995
Opitz GBBB syndrome: chromosomal evidence of an X-linked form
A Verloes, A David, S Odent, et al.
Prenatal Diagnosis
|
September 1, 1995
Fetal ascites and oligohydramnios: prenatal diagnosis of a sialic acid storage disease (index case)
P Poulain, S Odent, I Maire, et al.
Molecular Genetics and Metabolism
|
April 19, 2014
Involvement and alteration of the Sonic Hedgehog pathway is associated with decreased cholesterol level in trisomy 18 and SLO amniocytes
N Gruchy, N Bigot, C Jeanne Pasquier, et al.
Clinical Genetics
|
December 25, 2004
Sporadic optic atrophy due to synonymous codon change altering mRNA splicing of OPA1
P Amati-Bonneau, L Pasquier, E Lainey, et al.
Page
of 11
Search research articles
Search
Showing results (31-40 of 110) with videos related to
Sort By:
Page
of 11
Pediatrie
|
January 1, 1993
[Value and limits of autopsy in perinatal medicine. A plea for complete perimortem evaluation]
P Bétrémieux, P Pladys, P Poulain, et al.
Annales De Biologie Clinique
|
January 9, 2004
[Genetic study of holoprosencephaly]
C Dubourg, L Lazaro, M Blayau, et al.
Annales D'Endocrinologie
|
February 15, 2002
[Pseudohypoparathyroidism or hypoparathyroidism? A misleading clinical presentation]
C Derrien, S Odent, C Henry, et al.
American Journal of Medical Genetics
|
August 17, 1999
Paracentric inversion of the X chromosome [inv(X)(q12q28)] in familial FG syndrome
S Briault, S Odent, J Lucas, et al.
Pediatrie
|
January 1, 1993
[Diffuse subcortical heterotopias of the gray matter]
C Treguier, P Muh, C Le Berre, et al.
Journal of Assisted Reproduction and Genetics
|
November 13, 2014
Gene dosage effects in 46, XY DSD: usefulness of CGH technologies for diagnosis
S Jaillard, A Bashamboo, L Pasquier, et al.
American Journal of Medical Genetics
|
October 23, 1995
Opitz GBBB syndrome: chromosomal evidence of an X-linked form
A Verloes, A David, S Odent, et al.
Prenatal Diagnosis
|
September 1, 1995
Fetal ascites and oligohydramnios: prenatal diagnosis of a sialic acid storage disease (index case)
P Poulain, S Odent, I Maire, et al.
Molecular Genetics and Metabolism
|
April 19, 2014
Involvement and alteration of the Sonic Hedgehog pathway is associated with decreased cholesterol level in trisomy 18 and SLO amniocytes
N Gruchy, N Bigot, C Jeanne Pasquier, et al.
Clinical Genetics
|
December 25, 2004
Sporadic optic atrophy due to synonymous codon change altering mRNA splicing of OPA1
P Amati-Bonneau, L Pasquier, E Lainey, et al.
Page
of 11