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L Taine

Showing results (21-30 of 41) with videos related to

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Prenatal Diagnosis|January 1, 1996
Prenatal diagnosis in congenital erythropoietic porphyria by metabolic measurement and DNA mutation analysisC Ged, F Moreau-Gaudry, L Taine, et al.
Prenatal Diagnosis|January 1, 1994
Operator experience and fetal loss rate in transabdominal CVSR Saura, B Gauthier, L Taine, et al.
Genomics|November 1, 2000
Mapping, characterization, and expression analysis of the SM-20 human homologue, c1orf12, and identification of a novel related gene, SCAND2D Dupuy, I Aubert, V G Dupérat, et al.
Prenatal Diagnosis|October 1, 1993
Why confine chorionic villus biopsy to single pregnancies?R Saura, L Taine, J Horovitz, et al.
American Journal of Medical Genetics|December 20, 2000
Case with autistic syndrome and chromosome 22q13.3 deletion detected by FISHC Goizet, E Excoffier, L Taine, et al.
Genetic Counseling (Geneva, Switzerland)|April 7, 1999
Abdominal lymphatic dysplasia and 22q11 microdeletionT Mansir, D Lacombe, T Lamireau, et al.
Fetal Diagnosis and Therapy|November 6, 2001
Pregnancy outcome and prognosis in fetuses with increased first-trimester nuchal translucencyR Mangione, F Guyon, L Taine, et al.
The Journal of Gene Medicine|March 30, 2000
Fluorescence-based selection of retrovirally transduced cells in congenital erythropoietic porphyria: direct selection based on the expression of the therapeutic geneA Fontanellas, F Mazurier, F Belloc, et al.
American Journal of Medical Genetics|July 24, 1998
Submicroscopic deletion of chromosome 16p13.3 in patients with Rubinstein-Taybi syndromeL Taine, C Goizet, Z Q Wen, et al.
Prenatal Diagnosis|July 1, 1995
Prenatal diagnosis of trisomy 9. Six cases and a review of the literatureR Saura, W Traore, L Taine, et al.
Pageof 5

Showing results (21-30 of 41) with videos related to

Sort By:
Pageof 5
Prenatal Diagnosis|January 1, 1996
Prenatal diagnosis in congenital erythropoietic porphyria by metabolic measurement and DNA mutation analysisC Ged, F Moreau-Gaudry, L Taine, et al.
Prenatal Diagnosis|January 1, 1994
Operator experience and fetal loss rate in transabdominal CVSR Saura, B Gauthier, L Taine, et al.
Genomics|November 1, 2000
Mapping, characterization, and expression analysis of the SM-20 human homologue, c1orf12, and identification of a novel related gene, SCAND2D Dupuy, I Aubert, V G Dupérat, et al.
Prenatal Diagnosis|October 1, 1993
Why confine chorionic villus biopsy to single pregnancies?R Saura, L Taine, J Horovitz, et al.
American Journal of Medical Genetics|December 20, 2000
Case with autistic syndrome and chromosome 22q13.3 deletion detected by FISHC Goizet, E Excoffier, L Taine, et al.
Genetic Counseling (Geneva, Switzerland)|April 7, 1999
Abdominal lymphatic dysplasia and 22q11 microdeletionT Mansir, D Lacombe, T Lamireau, et al.
Fetal Diagnosis and Therapy|November 6, 2001
Pregnancy outcome and prognosis in fetuses with increased first-trimester nuchal translucencyR Mangione, F Guyon, L Taine, et al.
The Journal of Gene Medicine|March 30, 2000
Fluorescence-based selection of retrovirally transduced cells in congenital erythropoietic porphyria: direct selection based on the expression of the therapeutic geneA Fontanellas, F Mazurier, F Belloc, et al.
American Journal of Medical Genetics|July 24, 1998
Submicroscopic deletion of chromosome 16p13.3 in patients with Rubinstein-Taybi syndromeL Taine, C Goizet, Z Q Wen, et al.
Prenatal Diagnosis|July 1, 1995
Prenatal diagnosis of trisomy 9. Six cases and a review of the literatureR Saura, W Traore, L Taine, et al.
Pageof 5