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T Attie-Bitach

Showing results (1-10 of 12) with videos related to

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Ophthalmology|October 3, 2001
Renal coloboma syndromeP Dureau, T Attie-Bitach, R Salomon, et al.
Placenta|November 23, 2005
L-carnitine is synthesized in the human fetal-placental unit: potential roles in placental and fetal metabolismN A Oey, N van Vlies, F A Wijburg, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|June 28, 2021
Pathological and sonographic review of early isolated severe lower urinary tract obstruction and implications for prenatal treatmentN Vinit, B Bessières, E Spaggiari, et al.
Biochemical and Biophysical Research Communications|June 6, 2006
Acyl-CoA dehydrogenase 9 (ACAD 9) is the long-chain acyl-CoA dehydrogenase in human embryonic and fetal brainN A Oey, J P N Ruiter, L Ijlst, et al.
Eye (London, England)|January 16, 2010
New ocular phenotype associated with a mutation in the PAX2 geneF Beby, O Roche, P Cochat, et al.
Kidney International|February 13, 2001
PAX2 mutations in oligomeganephroniaR Salomon, A L Tellier, T Attie-Bitach, et al.
Journal of Medical Genetics|January 18, 2006
High throughput SNP and expression analyses of candidate genes for non-syndromic oral cleftsJ W Park, J Cai, I McIntosh, et al.
European Journal of Medical Genetics|July 29, 2009
Refining the clinicopathological pattern of cerebral proliferative glomeruloid vasculopathy (Fowler syndrome): report of 16 fetal casesB Bessières-Grattagliano, B Foliguet, L Devisme, et al.
Journal of Neuroradiology = Journal De Neuroradiologie|April 10, 2010
Posterior fossa imaging in 158 children with ataxiaN Boddaert, I Desguerre, N Bahi-Buisson, et al.
Journal of Medical Genetics|May 1, 2007
Genotype phenotype correlation of 30 patients with Smith-Magenis syndrome (SMS) using comparative genome hybridisation array: cleft palate in SMS is associated with larger deletionsJ Andrieux, C Villenet, S Quief, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Ophthalmology|October 3, 2001
Renal coloboma syndromeP Dureau, T Attie-Bitach, R Salomon, et al.
Placenta|November 23, 2005
L-carnitine is synthesized in the human fetal-placental unit: potential roles in placental and fetal metabolismN A Oey, N van Vlies, F A Wijburg, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|June 28, 2021
Pathological and sonographic review of early isolated severe lower urinary tract obstruction and implications for prenatal treatmentN Vinit, B Bessières, E Spaggiari, et al.
Biochemical and Biophysical Research Communications|June 6, 2006
Acyl-CoA dehydrogenase 9 (ACAD 9) is the long-chain acyl-CoA dehydrogenase in human embryonic and fetal brainN A Oey, J P N Ruiter, L Ijlst, et al.
Eye (London, England)|January 16, 2010
New ocular phenotype associated with a mutation in the PAX2 geneF Beby, O Roche, P Cochat, et al.
Kidney International|February 13, 2001
PAX2 mutations in oligomeganephroniaR Salomon, A L Tellier, T Attie-Bitach, et al.
Journal of Medical Genetics|January 18, 2006
High throughput SNP and expression analyses of candidate genes for non-syndromic oral cleftsJ W Park, J Cai, I McIntosh, et al.
European Journal of Medical Genetics|July 29, 2009
Refining the clinicopathological pattern of cerebral proliferative glomeruloid vasculopathy (Fowler syndrome): report of 16 fetal casesB Bessières-Grattagliano, B Foliguet, L Devisme, et al.
Journal of Neuroradiology = Journal De Neuroradiologie|April 10, 2010
Posterior fossa imaging in 158 children with ataxiaN Boddaert, I Desguerre, N Bahi-Buisson, et al.
Journal of Medical Genetics|May 1, 2007
Genotype phenotype correlation of 30 patients with Smith-Magenis syndrome (SMS) using comparative genome hybridisation array: cleft palate in SMS is associated with larger deletionsJ Andrieux, C Villenet, S Quief, et al.
Pageof 2