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Annales De Genetique
|
April 24, 1999
Congenital anomalies associated with congenital hypothyroidism
C Stoll, B Dott, Y Alembik, et al.
American Journal of Medical Genetics
|
July 3, 1995
Reply to Newton Freire-Maia on inbreeding among medical geneticists II
C Stoll, Y Alembik, B Dott, et al.
American Journal of Medical Genetics
|
January 1, 1994
Parental consanguinity as a cause of increased incidence of birth defects in a study of 131,760 consecutive births
C Stoll, Y Alembik, B Dott, et al.
Journal De Genetique Humaine
|
December 1, 1989
[Anomalies in thyroid function in children with trisomy 21]
C Stoll, Y Alembik, B Dott, et al.
Annales De Genetique
|
October 20, 1999
Parental consanguinity as a cause for increased incidence of births defects in a study of 238,942 consecutive births
C Stoll, Y Alembik, M P Roth, et al.
Journal of Medical Genetics
|
September 1, 1990
Genetic and environmental factors in hypospadias
C Stoll, Y Alembik, M P Roth, et al.
Archives Francaises De Pediatrie
|
November 1, 1988
[Etiologic and epidemiologic aspects of neural tube defects]
C Stoll, B Dott, M P Roth, et al.
Community Genetics
|
June 5, 2004
Study of 224 cases of oligohydramnios and congenital malformations in a series of 225,669 consecutive births
C Stoll, Y Alembik, M P Roth, et al.
Genetic Counseling (Geneva, Switzerland)
|
December 3, 2015
ASSOCIATED NON DIAPHRAGMATIC ANOMALIES AMONG CASES WITH CONGENITAL DIAPHRAGMATIC HERNIA
C Stoll, Y Alembik, B Dott, et al.
Archives Francaises De Pediatrie
|
March 1, 1987
[Congenital malformations in a series of 66,068 consecutive births]
M P Roth, B Dott, Y Alembik, et al.
Page
of 11
Search research articles
Search
Showing results (31-40 of 109) with videos related to
Sort By:
Page
of 11
Annales De Genetique
|
April 24, 1999
Congenital anomalies associated with congenital hypothyroidism
C Stoll, B Dott, Y Alembik, et al.
American Journal of Medical Genetics
|
July 3, 1995
Reply to Newton Freire-Maia on inbreeding among medical geneticists II
C Stoll, Y Alembik, B Dott, et al.
American Journal of Medical Genetics
|
January 1, 1994
Parental consanguinity as a cause of increased incidence of birth defects in a study of 131,760 consecutive births
C Stoll, Y Alembik, B Dott, et al.
Journal De Genetique Humaine
|
December 1, 1989
[Anomalies in thyroid function in children with trisomy 21]
C Stoll, Y Alembik, B Dott, et al.
Annales De Genetique
|
October 20, 1999
Parental consanguinity as a cause for increased incidence of births defects in a study of 238,942 consecutive births
C Stoll, Y Alembik, M P Roth, et al.
Journal of Medical Genetics
|
September 1, 1990
Genetic and environmental factors in hypospadias
C Stoll, Y Alembik, M P Roth, et al.
Archives Francaises De Pediatrie
|
November 1, 1988
[Etiologic and epidemiologic aspects of neural tube defects]
C Stoll, B Dott, M P Roth, et al.
Community Genetics
|
June 5, 2004
Study of 224 cases of oligohydramnios and congenital malformations in a series of 225,669 consecutive births
C Stoll, Y Alembik, M P Roth, et al.
Genetic Counseling (Geneva, Switzerland)
|
December 3, 2015
ASSOCIATED NON DIAPHRAGMATIC ANOMALIES AMONG CASES WITH CONGENITAL DIAPHRAGMATIC HERNIA
C Stoll, Y Alembik, B Dott, et al.
Archives Francaises De Pediatrie
|
March 1, 1987
[Congenital malformations in a series of 66,068 consecutive births]
M P Roth, B Dott, Y Alembik, et al.
Page
of 11