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C Stoll

Showing results (11-20 of 377) with videos related to

Pageof 38
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Human Genetics|January 1, 1981
Cytogenetic findings in 122 couples with recurrent abortionsC Stoll
Pathologie-Biologie|November 1, 1982
[Chromosomal abnormalities of the blastic phase of chronic myeloid leukemia]C Stoll
Genetic Counseling (Geneva, Switzerland)|January 13, 2000
Congenital blepharophimosis and ptosis in a mentally retarded girl: a new case of Ohdo syndrome?C Stoll
Nova Acta Paracelsica : ... Jahrbuch Der Schweizerischen Paracelsus-Gesellschaft|January 1, 1987
[Not Available]C Stoll
Human Genetics|January 1, 1980
Nonrandom distribution of exchange points in patients with reciprocal translocationsC Stoll
Genetic Counseling (Geneva, Switzerland)|July 23, 2003
Macrocephaly-cutis marmorata telangiectatica congenita: report of a patient with a translocationC Stoll
Pediatrie|September 1, 1985
[Opsomyoclonus syndrome in children. A new case. Review of the literature (110 cases)]P Talon, C Stoll
Annales De Genetique|July 18, 2002
Long-term follow-up of a girl with oro-facio-digital syndrome type I due to a mutation in the OFD 1 geneC Stoll, P Sauvage
Annales De Genetique|April 24, 1999
A syndrome of congenital ichthyosis, hypogonadism, small stature, facial dysmorphism, scoliosis and myogenic dystrophyC Stoll, D Eyer
Annales De Pediatrie|January 1, 1979
[Familial translocation t (16;19) (q24;q11) and birth of a girl with a trisomy 18]C Stoll, J Messer
Pageof 38

Showing results (11-20 of 377) with videos related to

Sort By:
Pageof 38
Human Genetics|January 1, 1981
Cytogenetic findings in 122 couples with recurrent abortionsC Stoll
Pathologie-Biologie|November 1, 1982
[Chromosomal abnormalities of the blastic phase of chronic myeloid leukemia]C Stoll
Genetic Counseling (Geneva, Switzerland)|January 13, 2000
Congenital blepharophimosis and ptosis in a mentally retarded girl: a new case of Ohdo syndrome?C Stoll
Nova Acta Paracelsica : ... Jahrbuch Der Schweizerischen Paracelsus-Gesellschaft|January 1, 1987
[Not Available]C Stoll
Human Genetics|January 1, 1980
Nonrandom distribution of exchange points in patients with reciprocal translocationsC Stoll
Genetic Counseling (Geneva, Switzerland)|July 23, 2003
Macrocephaly-cutis marmorata telangiectatica congenita: report of a patient with a translocationC Stoll
Pediatrie|September 1, 1985
[Opsomyoclonus syndrome in children. A new case. Review of the literature (110 cases)]P Talon, C Stoll
Annales De Genetique|July 18, 2002
Long-term follow-up of a girl with oro-facio-digital syndrome type I due to a mutation in the OFD 1 geneC Stoll, P Sauvage
Annales De Genetique|April 24, 1999
A syndrome of congenital ichthyosis, hypogonadism, small stature, facial dysmorphism, scoliosis and myogenic dystrophyC Stoll, D Eyer
Annales De Pediatrie|January 1, 1979
[Familial translocation t (16;19) (q24;q11) and birth of a girl with a trisomy 18]C Stoll, J Messer
Pageof 38