Search research articles
Contact Us
Filters
Showing results (61-70 of 112) with videos related to
Page
of 12
Sort By:
Human Molecular Genetics
|
June 1, 1994
Two novel rare frameshift mutations (2423 del G in exon 13 and 1215 del G in exon 7) and one novel rare sequence variation (3271 + 18 C or T) identified in a patient with cystic fibrosis
M C Romey, M Desgeorges, M Laussel, et al.
Annales De Genetique
|
January 1, 1989
[Diagnosis of minor chromosome modifications by molecular cytogenetics]
S Taviaux, A Moncla, F Giraud, et al.
Human Genetics
|
August 1, 1997
Cystic fibrosis in Lebanon: distribution of CFTR mutations among Arab communities
M Desgeorges, A Mégarbané, C Guittard, et al.
Genetic Counseling (Geneva, Switzerland)
|
January 1, 1997
An exonic polymorphism (381A/G) in the choroideremia gene
L Beaufrere, S Tuffery, C Hamel, et al.
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 boy
S Tuffery, P Moine, P Sarda, et al.
Prenatal Diagnosis
|
February 1, 1993
Prenatal diagnosis for cystic fibrosis using SSCP analysis
M Desgeorges, P Boulot, P Kjellberg, et al.
Journal Francais D'Ophtalmologie
|
January 1, 1997
[Rapid genetic diagnosis of females carriers related to patients with choroideremia]
L Beaufrère, S Tuffery, C Hamel, et al.
Developmental Biology
|
November 1, 1983
Evolution of Ca2+- and cAMP-dependent regulatory mechanisms during ram spermatogenesis
J Feinberg, C Pariset, M Rondard, et al.
American Journal of Medical Genetics. Part A
|
September 5, 2003
Identification of an autosomal recessive mode of inheritance in paediatric Behçet's families by segregation analysis
N Molinari, I Koné Paut, R Manna, et al.
Human Molecular Genetics
|
February 1, 1994
A novel splice site mutation in the first exon of the cystic fibrosis transmembrane regulator (CFTR) gene identified in a CBAVD patient
J F Culard, M Desgeorges, M C Romey, et al.
Page
of 12
Search research articles
Search
Showing results (61-70 of 112) with videos related to
Sort By:
Page
of 12
Human Molecular Genetics
|
June 1, 1994
Two novel rare frameshift mutations (2423 del G in exon 13 and 1215 del G in exon 7) and one novel rare sequence variation (3271 + 18 C or T) identified in a patient with cystic fibrosis
M C Romey, M Desgeorges, M Laussel, et al.
Annales De Genetique
|
January 1, 1989
[Diagnosis of minor chromosome modifications by molecular cytogenetics]
S Taviaux, A Moncla, F Giraud, et al.
Human Genetics
|
August 1, 1997
Cystic fibrosis in Lebanon: distribution of CFTR mutations among Arab communities
M Desgeorges, A Mégarbané, C Guittard, et al.
Genetic Counseling (Geneva, Switzerland)
|
January 1, 1997
An exonic polymorphism (381A/G) in the choroideremia gene
L Beaufrere, S Tuffery, C Hamel, et al.
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 boy
S Tuffery, P Moine, P Sarda, et al.
Prenatal Diagnosis
|
February 1, 1993
Prenatal diagnosis for cystic fibrosis using SSCP analysis
M Desgeorges, P Boulot, P Kjellberg, et al.
Journal Francais D'Ophtalmologie
|
January 1, 1997
[Rapid genetic diagnosis of females carriers related to patients with choroideremia]
L Beaufrère, S Tuffery, C Hamel, et al.
Developmental Biology
|
November 1, 1983
Evolution of Ca2+- and cAMP-dependent regulatory mechanisms during ram spermatogenesis
J Feinberg, C Pariset, M Rondard, et al.
American Journal of Medical Genetics. Part A
|
September 5, 2003
Identification of an autosomal recessive mode of inheritance in paediatric Behçet's families by segregation analysis
N Molinari, I Koné Paut, R Manna, et al.
Human Molecular Genetics
|
February 1, 1994
A novel splice site mutation in the first exon of the cystic fibrosis transmembrane regulator (CFTR) gene identified in a CBAVD patient
J F Culard, M Desgeorges, M C Romey, et al.
Page
of 12