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Annales De Genetique
|
January 1, 1997
Congenital eye malformations in 212,479 consecutive births
C Stoll, Y Alembik, B Dott, et al.
Clinical Genetics
|
November 1, 1980
Familial pterygium syndrome
C Stoll, J M Levy, P Kehr, et al.
Community Genetics
|
June 5, 2004
Study of 290 cases of polyhydramnios and congenital malformations in a series of 225,669 consecutive births
C G Stoll, M P Roth, B Dott, et al.
Pediatric Nephrology (Berlin, Germany)
|
July 1, 1990
Risk factors in internal urinary system malformations
C Stoll, Y Alembik, M P Roth, et al.
Human Genetics
|
December 1, 1995
Polymorphic tri- and tetranucleotide repeats in exons 1 and 8 of the myelin oligodendrocyte glycoprotein (MOG) gene
L Malfroy, C Viratelle, H Coppin, et al.
American Journal of Medical Genetics
|
February 1, 1985
Male-to-male transmission of the hypertelorism-hypospadias (BBB) syndrome
C Stoll, A Geraudel, H Berland, et al.
Prenatal Diagnosis
|
April 1, 1992
Evaluation of prenatal diagnosis by a registry of congenital anomalies
C Stoll, Y Alembik, B Dott, et al.
Archives Francaises De Pediatrie
|
October 1, 1991
[Congenital malformations in a series of 131,760 consecutive births during 10 years]
C Stoll, B Dott, Y Alembik, et al.
Human Genetics
|
January 1, 1983
Reexamination of paternal age effect in Down's syndrome
M P Roth, J Feingold, A Baumgarten, et al.
Clinical Genetics
|
September 1, 1985
A Weaver-like syndrome with endocrinological abnormalities in a boy and his mother
C Stoll, P Talon, L Mengus, et al.
Page
of 10
Search research articles
Search
Showing results (51-60 of 97) with videos related to
Sort By:
Page
of 10
Annales De Genetique
|
January 1, 1997
Congenital eye malformations in 212,479 consecutive births
C Stoll, Y Alembik, B Dott, et al.
Clinical Genetics
|
November 1, 1980
Familial pterygium syndrome
C Stoll, J M Levy, P Kehr, et al.
Community Genetics
|
June 5, 2004
Study of 290 cases of polyhydramnios and congenital malformations in a series of 225,669 consecutive births
C G Stoll, M P Roth, B Dott, et al.
Pediatric Nephrology (Berlin, Germany)
|
July 1, 1990
Risk factors in internal urinary system malformations
C Stoll, Y Alembik, M P Roth, et al.
Human Genetics
|
December 1, 1995
Polymorphic tri- and tetranucleotide repeats in exons 1 and 8 of the myelin oligodendrocyte glycoprotein (MOG) gene
L Malfroy, C Viratelle, H Coppin, et al.
American Journal of Medical Genetics
|
February 1, 1985
Male-to-male transmission of the hypertelorism-hypospadias (BBB) syndrome
C Stoll, A Geraudel, H Berland, et al.
Prenatal Diagnosis
|
April 1, 1992
Evaluation of prenatal diagnosis by a registry of congenital anomalies
C Stoll, Y Alembik, B Dott, et al.
Archives Francaises De Pediatrie
|
October 1, 1991
[Congenital malformations in a series of 131,760 consecutive births during 10 years]
C Stoll, B Dott, Y Alembik, et al.
Human Genetics
|
January 1, 1983
Reexamination of paternal age effect in Down's syndrome
M P Roth, J Feingold, A Baumgarten, et al.
Clinical Genetics
|
September 1, 1985
A Weaver-like syndrome with endocrinological abnormalities in a boy and his mother
C Stoll, P Talon, L Mengus, et al.
Page
of 10