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G Lefort

Showing results (71-80 of 114) with videos related to

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Genetic Counseling (Geneva, Switzerland)|January 1, 1994
Molecular diagnosis of Duchenne muscular dystrophy by use of a conformational polymorphism in the absence of DNA from an affected boyS Tuffery, P Moine, P Sarda, et al.
The Journal of Clinical Endocrinology and Metabolism|May 1, 1980
Congenital hypothyroidism associated with thyrotropin unresponsiveness and thyroid cell membrane alterationsJ L Codaccioni, P Carayon, M Michel-Bechet, et al.
Human Reproduction Update|April 14, 2011
Complex chromosomal rearrangements: origin and meiotic behaviorF Pellestor, T Anahory, G Lefort, et al.
Annales D'Endocrinologie|November 1, 1980
[The utilization of small repeated doses of iodine 131 in the treatment of Graves' disease. Results (author's transl)]J L Latapie, G Lefort, M Commenges, et al.
Journal of Medical Genetics|May 19, 2001
Cytogenetic and molecular study of a jumping translocation in a baby with Dandy-Walker malformationG Lefort, P Blanchet, A M Chaze, et al.
Gynecologic and Obstetric Investigation|January 1, 1993
Late vaginal induced abortion after a previous cesarean birth: potential for uterine ruptureP Boulot, M Hoffet, B Bachelard, et al.
Annales De Genetique|January 1, 1993
X-linked alpha-thalassemia/mental retardation (ATR-X) syndrome. Report of three male patients in a large French familyG Lefort, J Taib, A Toutain, et al.
La Nouvelle Presse Medicale|October 7, 1972
[Acute intermittent porphyria referred to a general surgery department]J M Coldefy, J Beurier, M Disdet, et al.
Annales De Genetique|January 1, 1995
[Direct analysis of the frequency of disomy in human sperm using the PRINS technique]I Quenesson, A Girardet, L Coignet, et al.
Prenatal Diagnosis|April 1, 1996
Prenatal aspects of giant fetal cranial haemangio-endotheliomaP Boulot, F Deschamps, F Montoya, et al.
Pageof 12

Showing results (71-80 of 114) with videos related to

Sort By:
Pageof 12
Genetic Counseling (Geneva, Switzerland)|January 1, 1994
Molecular diagnosis of Duchenne muscular dystrophy by use of a conformational polymorphism in the absence of DNA from an affected boyS Tuffery, P Moine, P Sarda, et al.
The Journal of Clinical Endocrinology and Metabolism|May 1, 1980
Congenital hypothyroidism associated with thyrotropin unresponsiveness and thyroid cell membrane alterationsJ L Codaccioni, P Carayon, M Michel-Bechet, et al.
Human Reproduction Update|April 14, 2011
Complex chromosomal rearrangements: origin and meiotic behaviorF Pellestor, T Anahory, G Lefort, et al.
Annales D'Endocrinologie|November 1, 1980
[The utilization of small repeated doses of iodine 131 in the treatment of Graves' disease. Results (author's transl)]J L Latapie, G Lefort, M Commenges, et al.
Journal of Medical Genetics|May 19, 2001
Cytogenetic and molecular study of a jumping translocation in a baby with Dandy-Walker malformationG Lefort, P Blanchet, A M Chaze, et al.
Gynecologic and Obstetric Investigation|January 1, 1993
Late vaginal induced abortion after a previous cesarean birth: potential for uterine ruptureP Boulot, M Hoffet, B Bachelard, et al.
Annales De Genetique|January 1, 1993
X-linked alpha-thalassemia/mental retardation (ATR-X) syndrome. Report of three male patients in a large French familyG Lefort, J Taib, A Toutain, et al.
La Nouvelle Presse Medicale|October 7, 1972
[Acute intermittent porphyria referred to a general surgery department]J M Coldefy, J Beurier, M Disdet, et al.
Annales De Genetique|January 1, 1995
[Direct analysis of the frequency of disomy in human sperm using the PRINS technique]I Quenesson, A Girardet, L Coignet, et al.
Prenatal Diagnosis|April 1, 1996
Prenatal aspects of giant fetal cranial haemangio-endotheliomaP Boulot, F Deschamps, F Montoya, et al.
Pageof 12