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Ferechte Encha-Razavi

Showing results (11-20 of 19) with videos related to

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American Journal of Human Genetics|December 14, 2004
Impaired mitochondrial glutamate transport in autosomal recessive neonatal myoclonic epilepsyFlorence Molinari, Annick Raas-Rothschild, Marlene Rio, et al.
Prenatal Diagnosis|July 13, 2019
SOX3 duplication: A genetic cause to investigate in fetuses with neural tube defectsMarguerite Hureaux, Selima Ben Miled, Nicolas Chatron, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 10, 2026
Spatiotemporal histogenesis of the developing human cerebellum reveals dynamic layering of Bergmann gliaGuanyi He, Simon Du, Henry Tan, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 18, 2025
Mapping the developmental profile of ventricular zone-derived neurons in the human cerebellumAnders W Erickson, Henry Tan, Liam D Hendrikse, et al.
American Journal of Medical Genetics|April 27, 2002
Cerebro-osseous-digital syndrome: four new cases of a lethal skeletal dysplasia--distinct from Neu-Laxova SyndromeAlison M Elliott, Marie Gonzales, Jean-Claude Hoeffel, et al.
American Journal of Human Genetics|December 13, 2006
The Meckel-Gruber syndrome gene, MKS3, is mutated in Joubert syndromeLekbir Baala, Stephane Romano, Rana Khaddour, et al.
American Journal of Obstetrics and Gynecology|April 14, 2020
Severe and progressive neuronal loss in myelomeningocele begins before 16 weeks of pregnancySelima Ben Miled, Laurence Loeuillet, Jean-Paul Duong Van Huyen, et al.
European Journal of Human Genetics : EJHG|April 17, 2014
New insights into genotype-phenotype correlation for GLI3 mutationsFlorence Démurger, Amale Ichkou, Soumaya Mougou-Zerelli, et al.
Human Molecular Genetics|December 10, 2013
Mutations in CNTNAP1 and ADCY6 are responsible for severe arthrogryposis multiplex congenita with axoglial defectsAnnie Laquérriere, Jérome Maluenda, Adrien Camus, et al.
Pageof 2

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
American Journal of Human Genetics|December 14, 2004
Impaired mitochondrial glutamate transport in autosomal recessive neonatal myoclonic epilepsyFlorence Molinari, Annick Raas-Rothschild, Marlene Rio, et al.
Prenatal Diagnosis|July 13, 2019
SOX3 duplication: A genetic cause to investigate in fetuses with neural tube defectsMarguerite Hureaux, Selima Ben Miled, Nicolas Chatron, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 10, 2026
Spatiotemporal histogenesis of the developing human cerebellum reveals dynamic layering of Bergmann gliaGuanyi He, Simon Du, Henry Tan, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 18, 2025
Mapping the developmental profile of ventricular zone-derived neurons in the human cerebellumAnders W Erickson, Henry Tan, Liam D Hendrikse, et al.
American Journal of Medical Genetics|April 27, 2002
Cerebro-osseous-digital syndrome: four new cases of a lethal skeletal dysplasia--distinct from Neu-Laxova SyndromeAlison M Elliott, Marie Gonzales, Jean-Claude Hoeffel, et al.
American Journal of Human Genetics|December 13, 2006
The Meckel-Gruber syndrome gene, MKS3, is mutated in Joubert syndromeLekbir Baala, Stephane Romano, Rana Khaddour, et al.
American Journal of Obstetrics and Gynecology|April 14, 2020
Severe and progressive neuronal loss in myelomeningocele begins before 16 weeks of pregnancySelima Ben Miled, Laurence Loeuillet, Jean-Paul Duong Van Huyen, et al.
European Journal of Human Genetics : EJHG|April 17, 2014
New insights into genotype-phenotype correlation for GLI3 mutationsFlorence Démurger, Amale Ichkou, Soumaya Mougou-Zerelli, et al.
Human Molecular Genetics|December 10, 2013
Mutations in CNTNAP1 and ADCY6 are responsible for severe arthrogryposis multiplex congenita with axoglial defectsAnnie Laquérriere, Jérome Maluenda, Adrien Camus, et al.
Pageof 2