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C Stoll

Showing results (141-150 of 377) with videos related to

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Fetal Diagnosis and Therapy|April 24, 2001
Different policies on prenatal ultrasound screening programmes and induced abortions explain regional variations in infant mortality with congenital malformationsE Garne, A Berghold, Z Johnson, et al.
American Journal of Medical Genetics|July 3, 1995
Reply to Newton Freire-Maia on inbreeding among medical geneticists IIC Stoll, Y Alembik, B Dott, et al.
Human Genetics|September 10, 1976
Familial 13p+ chromosome with mental retardation and dysmorphic features of two childrenC Stoll, A Rohmer, R Korn, 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 birthsC Stoll, Y Alembik, B Dott, et al.
Pediatrie|April 1, 1973
[Phenotypes of trisomy 13]C Stoll, D Willard, M Demay, et al.
Pediatrie|July 1, 1972
[A case of trisomy 18 with bilateral aplasia of the radius and thrombopenia]C Stoll, R Sacrez, D Willard, 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.
American Journal of Medical Genetics|August 26, 1998
A family with dominant oculoauriculovertebral spectrumC Stoll, B Viville, A Treisser, et al.
Human Genetics|March 12, 1979
Prenatal diagnosis and postnatal follow-up of an abnormal child with two de novo apparently balanced translocationsC Stoll, E Flori, J Macler, et al.
European Journal of Epidemiology|November 1, 1992
An epidemiologic study of environmental and genetic factors in congenital hydrocephalusC Stoll, Y Alembik, B Dott, et al.
Pageof 38

Showing results (141-150 of 377) with videos related to

Sort By:
Pageof 38
Fetal Diagnosis and Therapy|April 24, 2001
Different policies on prenatal ultrasound screening programmes and induced abortions explain regional variations in infant mortality with congenital malformationsE Garne, A Berghold, Z Johnson, et al.
American Journal of Medical Genetics|July 3, 1995
Reply to Newton Freire-Maia on inbreeding among medical geneticists IIC Stoll, Y Alembik, B Dott, et al.
Human Genetics|September 10, 1976
Familial 13p+ chromosome with mental retardation and dysmorphic features of two childrenC Stoll, A Rohmer, R Korn, 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 birthsC Stoll, Y Alembik, B Dott, et al.
Pediatrie|April 1, 1973
[Phenotypes of trisomy 13]C Stoll, D Willard, M Demay, et al.
Pediatrie|July 1, 1972
[A case of trisomy 18 with bilateral aplasia of the radius and thrombopenia]C Stoll, R Sacrez, D Willard, 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.
American Journal of Medical Genetics|August 26, 1998
A family with dominant oculoauriculovertebral spectrumC Stoll, B Viville, A Treisser, et al.
Human Genetics|March 12, 1979
Prenatal diagnosis and postnatal follow-up of an abnormal child with two de novo apparently balanced translocationsC Stoll, E Flori, J Macler, et al.
European Journal of Epidemiology|November 1, 1992
An epidemiologic study of environmental and genetic factors in congenital hydrocephalusC Stoll, Y Alembik, B Dott, et al.
Pageof 38