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Human Genetics
|
May 19, 1976
[A girl with a deletion (2) (q34q36): cytogenetic and clinical observations (author's transl)]
S Warter, C Lausecker, A Pennerath
Annales De Genetique
|
January 1, 1995
Autosomal recessive omodysplasia
C Stoll, A Pennerath, P Poirat
European Journal of Pediatrics
|
May 18, 1979
A girl with an end-to-end fusion of two X'S
C Stoll, C Lausecker, A Pennerath
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
November 1, 1995
[Spontaneous colonic perforations revealing Ehlers-Danlos syndrome type IV]
C Henry, S Geiss, E Wodey, et al.
Prenatal Diagnosis
|
September 22, 1998
Evaluation of prenatal diagnosis of congenital heart disease
C Stoll, Y Alembik, B Dott, et al.
Prenatal Diagnosis
|
July 1, 1997
Molecular analysis of the insulin receptor gene for prenatal diagnosis of leprechaunism in two families
C Desbois-Mouthon, E Girodon, N Ghanem, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 6) with videos related to
Sort By:
Page
of 1
Human Genetics
|
May 19, 1976
[A girl with a deletion (2) (q34q36): cytogenetic and clinical observations (author's transl)]
S Warter, C Lausecker, A Pennerath
Annales De Genetique
|
January 1, 1995
Autosomal recessive omodysplasia
C Stoll, A Pennerath, P Poirat
European Journal of Pediatrics
|
May 18, 1979
A girl with an end-to-end fusion of two X'S
C Stoll, C Lausecker, A Pennerath
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
November 1, 1995
[Spontaneous colonic perforations revealing Ehlers-Danlos syndrome type IV]
C Henry, S Geiss, E Wodey, et al.
Prenatal Diagnosis
|
September 22, 1998
Evaluation of prenatal diagnosis of congenital heart disease
C Stoll, Y Alembik, B Dott, et al.
Prenatal Diagnosis
|
July 1, 1997
Molecular analysis of the insulin receptor gene for prenatal diagnosis of leprechaunism in two families
C Desbois-Mouthon, E Girodon, N Ghanem, et al.
Page
of 1