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C Stoll

Showing results (61-70 of 377) with videos related to

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Genetic Counseling (Geneva, Switzerland)|January 1, 1995
Complex congenital heart disease, microcephaly, pheochromocytoma and neurofibromatosis type I in a girl born from consanguineous parentsC Stoll, Y Alembik, B Dott
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|January 1, 1992
[Evaluation of diagnostic technologies for congenital malformations]J Goujard, S Ayme, C Stoll
Journal of Orofacial Orthopedics = Fortschritte Der Kieferorthopadie : Organ/Official Journal Deutsche Gesellschaft Fur Kieferorthopadie|August 29, 2000
Nager syndrome. Problems and possibilities of therapyC Opitz, C Stoll, P Ring
Annales De Genetique|January 1, 1994
Association of Duane anomaly with mental retardation, cardiac and urinary tract abnormalities: a new autosomal recessive condition?C Stoll, Y Alembik, B Dott
Neurobiology of Disease|June 28, 2022
Leveraging the preformed fibril model to distinguish between alpha-synuclein inclusion- and nigrostriatal degeneration-associated immunogenicityAnna C Stoll, Caryl E Sortwell
Annales De Genetique|September 1, 1974
[Equilibrated 2-14 translocation in a mother and partial trisomy of a pair of the short branches of a number 2 chromosome in 2 of her children]C Stoll, J Messer, J Vors
Lancet (London, England)|February 24, 1973
X deletion and primary amenorrhoeaC Stoll, P Muller, P Dellenbach
Pediatrie|April 1, 1985
[Salmonella panama responsible for meningitis secondary to febrile gastroenteritis in a 3-month-old infant]P Talon, E Schneller, C Stoll
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
Clinical Genetics|October 1, 1996
Siblings with congenital renal tubular acidosis and nerve deafnessC Stoll, A Gentine, J Geisert
Pageof 38

Showing results (61-70 of 377) with videos related to

Sort By:
Pageof 38
Genetic Counseling (Geneva, Switzerland)|January 1, 1995
Complex congenital heart disease, microcephaly, pheochromocytoma and neurofibromatosis type I in a girl born from consanguineous parentsC Stoll, Y Alembik, B Dott
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|January 1, 1992
[Evaluation of diagnostic technologies for congenital malformations]J Goujard, S Ayme, C Stoll
Journal of Orofacial Orthopedics = Fortschritte Der Kieferorthopadie : Organ/Official Journal Deutsche Gesellschaft Fur Kieferorthopadie|August 29, 2000
Nager syndrome. Problems and possibilities of therapyC Opitz, C Stoll, P Ring
Annales De Genetique|January 1, 1994
Association of Duane anomaly with mental retardation, cardiac and urinary tract abnormalities: a new autosomal recessive condition?C Stoll, Y Alembik, B Dott
Neurobiology of Disease|June 28, 2022
Leveraging the preformed fibril model to distinguish between alpha-synuclein inclusion- and nigrostriatal degeneration-associated immunogenicityAnna C Stoll, Caryl E Sortwell
Annales De Genetique|September 1, 1974
[Equilibrated 2-14 translocation in a mother and partial trisomy of a pair of the short branches of a number 2 chromosome in 2 of her children]C Stoll, J Messer, J Vors
Lancet (London, England)|February 24, 1973
X deletion and primary amenorrhoeaC Stoll, P Muller, P Dellenbach
Pediatrie|April 1, 1985
[Salmonella panama responsible for meningitis secondary to febrile gastroenteritis in a 3-month-old infant]P Talon, E Schneller, C Stoll
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
Clinical Genetics|October 1, 1996
Siblings with congenital renal tubular acidosis and nerve deafnessC Stoll, A Gentine, J Geisert
Pageof 38