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D Bonneau

Showing results (121-130 of 143) with videos related to

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Diabetes & Metabolism|October 29, 2008
Mitochondrial DNA A3243G mutation involved in familial diabetes, chronic intestinal pseudo-obstruction and recurrent pancreatitisC Verny, P Amati-Bonneau, F Letournel, et al.
Pathologie-Biologie|February 2, 2010
[Genetic testing in the context of the revision of the French law on bioethics]D Bonneau, S Marlin, D Sanlaville, et al.
European Journal of Human Genetics : EJHG|May 1, 1997
A YAC contig spanning the blepharophimosis-ptosis-epicanthus inversus syndrome and propionic acidemia lociM R Piemontese, E Memeo, M Carella, et al.
British Journal of Cancer|May 29, 2008
Prognostic molecular markers with no impact on decision-making: the paradox of gliomas based on a prospective studyM Wager, P Menei, J Guilhot, et al.
JIMD Reports|February 23, 2013
Kinetic analyses guide the therapeutic decision in a novel form of moderate aromatic Acid decarboxylase deficiencyM Barth, V Serre, L Hubert, et al.
Clinical Genetics|May 29, 2010
C2orf37 mutational spectrum in Woodhouse-Sakati syndrome patientsA M Alazami, S A Schneider, D Bonneau, et al.
Clinical Genetics|December 1, 1996
Increased paternal age in CHARGE associationA L Tellier, S Lyonnet, V Cormier-Daire, et al.
Journal of Medical Genetics|November 3, 2004
PTPN11 mutations in patients with LEOPARD syndrome: a French multicentric experienceB Keren, A Hadchouel, S Saba, et al.
Molecular Genetics and Metabolism Reports|April 17, 2025
The recurrent p.Glu3Lys variant in <i>EHHADH</i> is responsible for Fanconi syndrome with early liver dysfunction and mitochondrial abnormalitiesP Rollier, A Cospain, M Barth, et al.
Journal of Medical Genetics|September 3, 2004
OPA3 gene mutations responsible for autosomal dominant optic atrophy and cataractP Reynier, P Amati-Bonneau, C Verny, et al.
Pageof 15

Showing results (121-130 of 143) with videos related to

Sort By:
Pageof 15
Diabetes & Metabolism|October 29, 2008
Mitochondrial DNA A3243G mutation involved in familial diabetes, chronic intestinal pseudo-obstruction and recurrent pancreatitisC Verny, P Amati-Bonneau, F Letournel, et al.
Pathologie-Biologie|February 2, 2010
[Genetic testing in the context of the revision of the French law on bioethics]D Bonneau, S Marlin, D Sanlaville, et al.
European Journal of Human Genetics : EJHG|May 1, 1997
A YAC contig spanning the blepharophimosis-ptosis-epicanthus inversus syndrome and propionic acidemia lociM R Piemontese, E Memeo, M Carella, et al.
British Journal of Cancer|May 29, 2008
Prognostic molecular markers with no impact on decision-making: the paradox of gliomas based on a prospective studyM Wager, P Menei, J Guilhot, et al.
JIMD Reports|February 23, 2013
Kinetic analyses guide the therapeutic decision in a novel form of moderate aromatic Acid decarboxylase deficiencyM Barth, V Serre, L Hubert, et al.
Clinical Genetics|May 29, 2010
C2orf37 mutational spectrum in Woodhouse-Sakati syndrome patientsA M Alazami, S A Schneider, D Bonneau, et al.
Clinical Genetics|December 1, 1996
Increased paternal age in CHARGE associationA L Tellier, S Lyonnet, V Cormier-Daire, et al.
Journal of Medical Genetics|November 3, 2004
PTPN11 mutations in patients with LEOPARD syndrome: a French multicentric experienceB Keren, A Hadchouel, S Saba, et al.
Molecular Genetics and Metabolism Reports|April 17, 2025
The recurrent p.Glu3Lys variant in <i>EHHADH</i> is responsible for Fanconi syndrome with early liver dysfunction and mitochondrial abnormalitiesP Rollier, A Cospain, M Barth, et al.
Journal of Medical Genetics|September 3, 2004
OPA3 gene mutations responsible for autosomal dominant optic atrophy and cataractP Reynier, P Amati-Bonneau, C Verny, et al.
Pageof 15