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Y Alembik

Showing results (11-20 of 109) with videos related to

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Genetic Counseling (Geneva, Switzerland)|January 1, 1994
A syndrome of facial dysmorphia, birth defects, myelodysplasia and immunodeficiency in three sibs of consanguineous parentsC Stoll, Y Alembik, P Lutz
Genetic Counseling (Geneva, Switzerland)|August 23, 2007
Associated malformations in cases with neural tube defectsC Stoll, Y Alembik, B Dott
Genetic Counseling (Geneva, Switzerland)|January 1, 1997
On the phenotypic overlap between "severe" oto-palato digital type II syndrome and Larsen syndrome. Variable manifestation of a single autosomal dominant geneY Alembik, C Stoll, J Messer
Annales De Genetique|October 20, 1999
Familial coarctation of the aorta in three generationsC Stoll, Y Alembik, B Dott
Annales De Genetique|January 1, 1996
Multiple familial lipomatosis with polyneuropathy, an inherited dominant conditionC Stoll, Y Alembik, M Truttmann
Genetic Counseling (Geneva, Switzerland)|April 29, 1998
Oligodontia, microcephaly and facial dysmorphia syndromeC Stoll, B Dott, Y Alembik
Genetic Counseling (Geneva, Switzerland)|July 17, 1998
Congenital bilateral fibular deficiency with facial dysmorphia, brachydactyly and mental retardation in a girlC Stoll, Y Alembik, M Repetto
European Journal of Medical Genetics|August 1, 2006
Are the recommendations on the prevention of neural tube defects working?C Stoll, Y Alembik, B Dott
Annales De Genetique|January 1, 1996
Familial distal arthrogryposis type IC Stoll, Y Alembik, B Dott
American Journal of Obstetrics and Gynecology|September 1, 1991
Study of 156 cases of polyhydramnios and congenital malformations in a series of 118,265 consecutive birthsC G Stoll, Y Alembik, B Dott
Pageof 11

Showing results (11-20 of 109) with videos related to

Sort By:
Pageof 11
Genetic Counseling (Geneva, Switzerland)|January 1, 1994
A syndrome of facial dysmorphia, birth defects, myelodysplasia and immunodeficiency in three sibs of consanguineous parentsC Stoll, Y Alembik, P Lutz
Genetic Counseling (Geneva, Switzerland)|August 23, 2007
Associated malformations in cases with neural tube defectsC Stoll, Y Alembik, B Dott
Genetic Counseling (Geneva, Switzerland)|January 1, 1997
On the phenotypic overlap between "severe" oto-palato digital type II syndrome and Larsen syndrome. Variable manifestation of a single autosomal dominant geneY Alembik, C Stoll, J Messer
Annales De Genetique|October 20, 1999
Familial coarctation of the aorta in three generationsC Stoll, Y Alembik, B Dott
Annales De Genetique|January 1, 1996
Multiple familial lipomatosis with polyneuropathy, an inherited dominant conditionC Stoll, Y Alembik, M Truttmann
Genetic Counseling (Geneva, Switzerland)|April 29, 1998
Oligodontia, microcephaly and facial dysmorphia syndromeC Stoll, B Dott, Y Alembik
Genetic Counseling (Geneva, Switzerland)|July 17, 1998
Congenital bilateral fibular deficiency with facial dysmorphia, brachydactyly and mental retardation in a girlC Stoll, Y Alembik, M Repetto
European Journal of Medical Genetics|August 1, 2006
Are the recommendations on the prevention of neural tube defects working?C Stoll, Y Alembik, B Dott
Annales De Genetique|January 1, 1996
Familial distal arthrogryposis type IC Stoll, Y Alembik, B Dott
American Journal of Obstetrics and Gynecology|September 1, 1991
Study of 156 cases of polyhydramnios and congenital malformations in a series of 118,265 consecutive birthsC G Stoll, Y Alembik, B Dott
Pageof 11