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M Lobaccaro

Showing results (11-20 of 51) with videos related to

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Human Molecular Genetics|July 1, 1993
An exonic point mutation creates a MaeIII site in the androgen receptor gene of a family with complete androgen insensitivity syndromeJ M Lobaccaro, S Lumbroso, R Ktari, et al.
Hormone Research|January 1, 1992
Molecular biology of disorders of sex differentiationC Sultan, J M Lobaccaro, C Belon, et al.
Molecular and Cellular Endocrinology|June 20, 1997
Functional and structural analysis of R607Q and R608K androgen receptor substitutions associated with male breast cancerN Poujol, J M Lobaccaro, L Chiche, et al.
Cellular and Molecular Biology (Noisy-Le-Grand, France)|May 1, 1994
Molecular genetics of androgen insensitivity syndromesJ M Lobaccaro, S Lumbroso, N Poujol, et al.
The Journal of Steroid Biochemistry and Molecular Biology|March 1, 1993
Complete androgen insensitivity syndrome associated with a de novo mutation of the androgen receptor gene detected by single strand conformation polymorphismJ M Lobaccaro, S Lumbroso, P Berta, et al.
Annales D'Endocrinologie|January 1, 1994
[Genes of the Y chromosome and Turner syndrome]J M Lobaccaro, S Lumbroso, C Belon, et al.
The Journal of Steroid Biochemistry and Molecular Biology|November 1, 1993
Mutations of androgen receptor gene in androgen insensitivity syndromesC Sultan, S Lumbroso, N Poujol, et al.
Fertility and Sterility|November 1, 1993
A new mutation within the deoxyribonucleic acid-binding domain of the androgen receptor gene in a family with complete androgen insensitivity syndromeS Lumbroso, J M Lobaccaro, C Belon, et al.
Molecular and Cellular Endocrinology|February 5, 1996
Molecular modeling and in vitro investigations of the human androgen receptor DNA-binding domain: application for the study of two mutationsJ M Lobaccaro, N Poujol, L Chiche, et al.
Human Genetics|December 1, 1990
Defective, deleted or converted CYP21B gene and negative association with a rare restriction fragment length polymorphism allele of the factor B gene in congenital adrenal hyperplasiaN Ghanem, J M Lobaccaro, C Buresi, et al.
Pageof 6

Showing results (11-20 of 51) with videos related to

Sort By:
Pageof 6
Human Molecular Genetics|July 1, 1993
An exonic point mutation creates a MaeIII site in the androgen receptor gene of a family with complete androgen insensitivity syndromeJ M Lobaccaro, S Lumbroso, R Ktari, et al.
Hormone Research|January 1, 1992
Molecular biology of disorders of sex differentiationC Sultan, J M Lobaccaro, C Belon, et al.
Molecular and Cellular Endocrinology|June 20, 1997
Functional and structural analysis of R607Q and R608K androgen receptor substitutions associated with male breast cancerN Poujol, J M Lobaccaro, L Chiche, et al.
Cellular and Molecular Biology (Noisy-Le-Grand, France)|May 1, 1994
Molecular genetics of androgen insensitivity syndromesJ M Lobaccaro, S Lumbroso, N Poujol, et al.
The Journal of Steroid Biochemistry and Molecular Biology|March 1, 1993
Complete androgen insensitivity syndrome associated with a de novo mutation of the androgen receptor gene detected by single strand conformation polymorphismJ M Lobaccaro, S Lumbroso, P Berta, et al.
Annales D'Endocrinologie|January 1, 1994
[Genes of the Y chromosome and Turner syndrome]J M Lobaccaro, S Lumbroso, C Belon, et al.
The Journal of Steroid Biochemistry and Molecular Biology|November 1, 1993
Mutations of androgen receptor gene in androgen insensitivity syndromesC Sultan, S Lumbroso, N Poujol, et al.
Fertility and Sterility|November 1, 1993
A new mutation within the deoxyribonucleic acid-binding domain of the androgen receptor gene in a family with complete androgen insensitivity syndromeS Lumbroso, J M Lobaccaro, C Belon, et al.
Molecular and Cellular Endocrinology|February 5, 1996
Molecular modeling and in vitro investigations of the human androgen receptor DNA-binding domain: application for the study of two mutationsJ M Lobaccaro, N Poujol, L Chiche, et al.
Human Genetics|December 1, 1990
Defective, deleted or converted CYP21B gene and negative association with a rare restriction fragment length polymorphism allele of the factor B gene in congenital adrenal hyperplasiaN Ghanem, J M Lobaccaro, C Buresi, et al.
Pageof 6