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Genetic Counseling (Geneva, Switzerland)
|
November 11, 2008
Associated malformations in cases with congenital diaphragmatic hernia
C Stoll, Y Alembik, B Dott, et al.
American Journal of Medical Genetics
|
June 19, 1998
Classification of limb defects
C Stoll, D Duboule, L B Holmes, et al.
Annales De Genetique
|
May 26, 1998
Study of Down syndrome in 238,942 consecutive births
C Stoll, Y Alembik, B Dott, et al.
Annales De Genetique
|
January 1, 1997
Risk factors in congenital anal atresias
C Stoll, Y Alembik, M P Roth, et al.
Prenatal Diagnosis
|
November 1, 1985
Prenatal diagnosis of hypochondroplasia
C Stoll, P Manini, J Bloch, et al.
Journal of Medical Genetics
|
May 1, 1991
Epidemiological and genetic study in 207 cases of oral clefts in Alsace, north-eastern France
C Stoll, Y Alembik, B Dott, et al.
Genetic Counseling (Geneva, Switzerland)
|
January 1, 1997
Brachydactyly and short stature in a mother and her daughter with a fragile site at 16q22
C Stoll, B Roy-Doray, B Dott, et al.
Annales De Genetique
|
April 6, 2002
Evaluation and evolution during time of prenatal diagnosis of congenital heart diseases by routine fetal ultrasonographic examination
C Stoll, B Dott, Y Alembik, et al.
Annals of Internal Medicine
|
August 1, 1975
Letter: Duplication of Philadelphia chromosome in acute transition of chronic granulocytic leukaemia
F Oberling, C Stoll, J M Lang, et al.
Nouvelle Revue Francaise D'Hematologie
|
January 1, 1976
[Clinics and genetics of Glanzmann's thrombasthenia (author's translation)]
J M Lévy, C Stoll, A Gardea, et al.
Page
of 38
Search research articles
Search
Showing results (181-190 of 377) with videos related to
Sort By:
Page
of 38
Genetic Counseling (Geneva, Switzerland)
|
November 11, 2008
Associated malformations in cases with congenital diaphragmatic hernia
C Stoll, Y Alembik, B Dott, et al.
American Journal of Medical Genetics
|
June 19, 1998
Classification of limb defects
C Stoll, D Duboule, L B Holmes, et al.
Annales De Genetique
|
May 26, 1998
Study of Down syndrome in 238,942 consecutive births
C Stoll, Y Alembik, B Dott, et al.
Annales De Genetique
|
January 1, 1997
Risk factors in congenital anal atresias
C Stoll, Y Alembik, M P Roth, et al.
Prenatal Diagnosis
|
November 1, 1985
Prenatal diagnosis of hypochondroplasia
C Stoll, P Manini, J Bloch, et al.
Journal of Medical Genetics
|
May 1, 1991
Epidemiological and genetic study in 207 cases of oral clefts in Alsace, north-eastern France
C Stoll, Y Alembik, B Dott, et al.
Genetic Counseling (Geneva, Switzerland)
|
January 1, 1997
Brachydactyly and short stature in a mother and her daughter with a fragile site at 16q22
C Stoll, B Roy-Doray, B Dott, et al.
Annales De Genetique
|
April 6, 2002
Evaluation and evolution during time of prenatal diagnosis of congenital heart diseases by routine fetal ultrasonographic examination
C Stoll, B Dott, Y Alembik, et al.
Annals of Internal Medicine
|
August 1, 1975
Letter: Duplication of Philadelphia chromosome in acute transition of chronic granulocytic leukaemia
F Oberling, C Stoll, J M Lang, et al.
Nouvelle Revue Francaise D'Hematologie
|
January 1, 1976
[Clinics and genetics of Glanzmann's thrombasthenia (author's translation)]
J M Lévy, C Stoll, A Gardea, et al.
Page
of 38