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Damien Sanlaville

Showing results (1-10 of 231) with videos related to

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European Journal of Human Genetics : EJHG|February 15, 2007
CHARGE syndrome: an updateDamien Sanlaville, Alain Verloes
La Revue Du Praticien|May 10, 2011
[Genetic tools]Nadia Boutry-Kryza, Damien Sanlaville
Medecine Sciences : M/S|October 7, 2020
[Microlissencephaly due to pathogenic variants of NDE1: from pathology to normal brain development]Sara Cabet, Laurent Guibaud, Damien Sanlaville
Orphanet Journal of Rare Diseases|February 24, 2009
Distal Xq duplication and functional Xq disomyDamien Sanlaville, Caroline Schluth-Bolard, Catherine Turleau
Acta Paediatrica (Oslo, Norway : 1992)|December 15, 2015
Milk kinship is not an obstacle to using donor human milk to feed preterm infants in Muslim countriesAliaa Khalil, Rachel Buffin, Damien Sanlaville, et al.
Medecine Sciences : M/S|November 15, 2006
[Contiguous gene deletion within chromosome arm 10q is associated with juvenile polyposis of infancy, reflecting cooperation between the BMPR1A and PTEN tumor-suppressor genes]Capucine Delnatte, Damien Sanlaville, Jean-François Mougenot, et al.
La Revue Du Praticien|February 11, 2022
[French Genomic Medicine Plan 2025 (PFMG2025): France enters the era of genomic medicine]Damien Sanlaville, Michel Vidaud, Christel Thauvin-Robinet, et al.
American Journal of Medical Genetics. Part A|March 27, 2014
A new intellectual disability syndrome caused by CTNNB1 haploinsufficiencyEstelle Dubruc, Audrey Putoux, Audrey Labalme, et al.
Journal of Pediatric Gastroenterology and Nutrition|December 31, 2005
Heterozygous bile salt export pump deficiency: a possible genetic predisposition to transient neonatal cholestasisBogdan Hermeziu, Damien Sanlaville, Muriel Girard, et al.
Pediatric Nephrology (Berlin, Germany)|June 29, 2023
Kidney and urological involvement in Down syndrome: frequent, underestimated, but associated with impaired quality of life and risk of kidney failureBruno Ranchin, Valeska Bidault, Franck Zekre, et al.
Pageof 24

Showing results (1-10 of 231) with videos related to

Sort By:
Pageof 24
European Journal of Human Genetics : EJHG|February 15, 2007
CHARGE syndrome: an updateDamien Sanlaville, Alain Verloes
La Revue Du Praticien|May 10, 2011
[Genetic tools]Nadia Boutry-Kryza, Damien Sanlaville
Medecine Sciences : M/S|October 7, 2020
[Microlissencephaly due to pathogenic variants of NDE1: from pathology to normal brain development]Sara Cabet, Laurent Guibaud, Damien Sanlaville
Orphanet Journal of Rare Diseases|February 24, 2009
Distal Xq duplication and functional Xq disomyDamien Sanlaville, Caroline Schluth-Bolard, Catherine Turleau
Acta Paediatrica (Oslo, Norway : 1992)|December 15, 2015
Milk kinship is not an obstacle to using donor human milk to feed preterm infants in Muslim countriesAliaa Khalil, Rachel Buffin, Damien Sanlaville, et al.
Medecine Sciences : M/S|November 15, 2006
[Contiguous gene deletion within chromosome arm 10q is associated with juvenile polyposis of infancy, reflecting cooperation between the BMPR1A and PTEN tumor-suppressor genes]Capucine Delnatte, Damien Sanlaville, Jean-François Mougenot, et al.
La Revue Du Praticien|February 11, 2022
[French Genomic Medicine Plan 2025 (PFMG2025): France enters the era of genomic medicine]Damien Sanlaville, Michel Vidaud, Christel Thauvin-Robinet, et al.
American Journal of Medical Genetics. Part A|March 27, 2014
A new intellectual disability syndrome caused by CTNNB1 haploinsufficiencyEstelle Dubruc, Audrey Putoux, Audrey Labalme, et al.
Journal of Pediatric Gastroenterology and Nutrition|December 31, 2005
Heterozygous bile salt export pump deficiency: a possible genetic predisposition to transient neonatal cholestasisBogdan Hermeziu, Damien Sanlaville, Muriel Girard, et al.
Pediatric Nephrology (Berlin, Germany)|June 29, 2023
Kidney and urological involvement in Down syndrome: frequent, underestimated, but associated with impaired quality of life and risk of kidney failureBruno Ranchin, Valeska Bidault, Franck Zekre, et al.
Pageof 24