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S Lyonnet

Showing results (41-50 of 223) with videos related to

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Pathologie-Biologie|January 14, 1999
[From monogenic to polygenic: model of Hirschsprung disease]R Salomon, J Amiel, T Attié, et al.
European Journal of Biochemistry|July 15, 1987
Dietary and hormonal regulation of L-type pyruvate kinase gene expression in rat small intestineH Ogier, A Munnich, S Lyonnet, et al.
Bulletin Du Cancer|April 1, 1996
[Severe 5-fluorouracil toxicity in a woman treated for breast cancer with concurrent osteogenesis imperfecta and dehydrogenase deficiency]P Beuzeboc, J Y Pierga, D S Lyonnet, et al.
Prenatal Diagnosis|September 1, 1991
First-trimester prenatal diagnosis in quintuplets: a practical approach using step-by-step embryo reductionY Dumez, M Dommergues, S Lyonnet, et al.
Journal of Medical Genetics|October 1, 1991
An animal model for maternal phenylketonuriaC Roux, F Rey, S Lyonnet, et al.
Journal of Medical Genetics|July 29, 1999
Epiphyseal, vertebral, and ear (EVE) dysplasia: a new syndrome?J Amiel, V Cormier-Daire, P Journeau, et al.
The Journal of Pediatrics|April 11, 2001
Prevalence of 22q11 deletion in fetuses with conotruncal cardiac defects: a 6-year prospective studyY Boudjemline, L Fermont, J Le Bidois, et al.
Clinical Genetics|August 18, 1999
Dysmorphic phenotype and neurological impairment in 22 retinoblastoma patients with constitutional cytogenetic 13q deletionO Baud, V Cormier-Daire, S Lyonnet, et al.
Human Mutation|April 29, 1999
Co-segregation of MEN2 and Hirschsprung's disease: the same mutation of RET with both gain and loss-of-function?M Takahashi, T Iwashita, M Santoro, et al.
The Journal of Clinical Endocrinology and Metabolism|May 10, 2001
Nineteen years of national screening for congenital hypothyroidism: familial cases with thyroid dysgenesis suggest the involvement of genetic factorsM Castanet, M Polak, C Bonaïti-Pellié, et al.
Pageof 23

Showing results (41-50 of 223) with videos related to

Sort By:
Pageof 23
Pathologie-Biologie|January 14, 1999
[From monogenic to polygenic: model of Hirschsprung disease]R Salomon, J Amiel, T Attié, et al.
European Journal of Biochemistry|July 15, 1987
Dietary and hormonal regulation of L-type pyruvate kinase gene expression in rat small intestineH Ogier, A Munnich, S Lyonnet, et al.
Bulletin Du Cancer|April 1, 1996
[Severe 5-fluorouracil toxicity in a woman treated for breast cancer with concurrent osteogenesis imperfecta and dehydrogenase deficiency]P Beuzeboc, J Y Pierga, D S Lyonnet, et al.
Prenatal Diagnosis|September 1, 1991
First-trimester prenatal diagnosis in quintuplets: a practical approach using step-by-step embryo reductionY Dumez, M Dommergues, S Lyonnet, et al.
Journal of Medical Genetics|October 1, 1991
An animal model for maternal phenylketonuriaC Roux, F Rey, S Lyonnet, et al.
Journal of Medical Genetics|July 29, 1999
Epiphyseal, vertebral, and ear (EVE) dysplasia: a new syndrome?J Amiel, V Cormier-Daire, P Journeau, et al.
The Journal of Pediatrics|April 11, 2001
Prevalence of 22q11 deletion in fetuses with conotruncal cardiac defects: a 6-year prospective studyY Boudjemline, L Fermont, J Le Bidois, et al.
Clinical Genetics|August 18, 1999
Dysmorphic phenotype and neurological impairment in 22 retinoblastoma patients with constitutional cytogenetic 13q deletionO Baud, V Cormier-Daire, S Lyonnet, et al.
Human Mutation|April 29, 1999
Co-segregation of MEN2 and Hirschsprung's disease: the same mutation of RET with both gain and loss-of-function?M Takahashi, T Iwashita, M Santoro, et al.
The Journal of Clinical Endocrinology and Metabolism|May 10, 2001
Nineteen years of national screening for congenital hypothyroidism: familial cases with thyroid dysgenesis suggest the involvement of genetic factorsM Castanet, M Polak, C Bonaïti-Pellié, et al.
Pageof 23