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C Stoll

Showing results (71-80 of 377) with videos related to

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Journal De Genetique Humaine|September 1, 1980
[Echographic detection of fetal malformations (experience of an At-risk Pregnancy Center)]J Macler, C Stoll, R Renaud
Annales De Genetique|January 1, 1996
Familial distal arthrogryposis type IC Stoll, Y Alembik, B Dott
Annales De Genetique|September 1, 1973
[22-ring chromosome: identification by controlled heat denaturation]C Stoll, A Rohmer, P Sauvage
Genetic Counseling (Geneva, Switzerland)|January 13, 2000
A three generations family with blepharo-naso-facial malformations suggestive of Pashayan syndromeC Stoll, J Terzic, M Fischbach
Community Genetics|July 11, 2002
Detection of Congenital Anomalies by Fetal Ultrasonographic Examination across EuropeC. Stoll, R. Tenconi, M. Clementi
Annales De Genetique|January 1, 1995
Autosomal recessive omodysplasiaC Stoll, A Pennerath, P Poirat
Prenatal Diagnosis|April 5, 2001
Evaluation of prenatal diagnosis of associated congenital heart diseases by fetal ultrasonographic examination in EuropeC Stoll, E Garne, M Clementi, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1995
Rett-like syndrome in fragile X syndromeY Alembik, B Dott, C Stoll
Blood|October 1, 1978
Chromosome analysis of spleen and/or lymph nodes of patients with chronic myeloid leukemia (CML)C Stoll, F Oberling, E Flori
Annales De Genetique|December 9, 2003
Limb reduction defects in the first generation and deafness in the second generation of intrauterine exposed fetuses to diethylstilbestrolC Stoll, Y Alembik, B Dott
Pageof 38

Showing results (71-80 of 377) with videos related to

Sort By:
Pageof 38
Journal De Genetique Humaine|September 1, 1980
[Echographic detection of fetal malformations (experience of an At-risk Pregnancy Center)]J Macler, C Stoll, R Renaud
Annales De Genetique|January 1, 1996
Familial distal arthrogryposis type IC Stoll, Y Alembik, B Dott
Annales De Genetique|September 1, 1973
[22-ring chromosome: identification by controlled heat denaturation]C Stoll, A Rohmer, P Sauvage
Genetic Counseling (Geneva, Switzerland)|January 13, 2000
A three generations family with blepharo-naso-facial malformations suggestive of Pashayan syndromeC Stoll, J Terzic, M Fischbach
Community Genetics|July 11, 2002
Detection of Congenital Anomalies by Fetal Ultrasonographic Examination across EuropeC. Stoll, R. Tenconi, M. Clementi
Annales De Genetique|January 1, 1995
Autosomal recessive omodysplasiaC Stoll, A Pennerath, P Poirat
Prenatal Diagnosis|April 5, 2001
Evaluation of prenatal diagnosis of associated congenital heart diseases by fetal ultrasonographic examination in EuropeC Stoll, E Garne, M Clementi, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1995
Rett-like syndrome in fragile X syndromeY Alembik, B Dott, C Stoll
Blood|October 1, 1978
Chromosome analysis of spleen and/or lymph nodes of patients with chronic myeloid leukemia (CML)C Stoll, F Oberling, E Flori
Annales De Genetique|December 9, 2003
Limb reduction defects in the first generation and deafness in the second generation of intrauterine exposed fetuses to diethylstilbestrolC Stoll, Y Alembik, B Dott
Pageof 38