Search research articles
Contact Us
Filters
Showing results (181-190 of 284) with videos related to
Page
of 29
Sort By:
Annales De Medecine Interne
|
November 1, 1977
[Generalized saturnine paralysis. Discovery of a double congenital disease: glucose-6-phosphate dehydrogenase deficiency (new variant) and distal tubular acidosis]
F Nouailhat, J C Kaplan, Y Giudicelli, et al.
Human Genetics
|
July 7, 1976
Gene dosage effect in human triploid fibroblasts
C Junien, H Rubinson, J C Dreyfus, et al.
Cancer Research
|
July 1, 1995
Seven megabase yeast artificial chromosome contig at region 11p15: identification of a yeast artificial chromosome spanning the breakpoint of a chromosomal translocation found in a case of Beckwith-Wiedemann syndrome
M Negrini, S Sabbioni, M Ohta, et al.
Annales De Genetique
|
January 1, 1982
Inverted tandem duplication of the short arm of chromosome 8: a non-random de novo structural aberration in man. Localization of the gene for glutathione reductase in subband 8p21.1
P K Jensen, C Junien, S Despoisse, et al.
Human Genetics
|
July 1, 1991
Recurrent mutation at aa 792 in the LDL receptor gene in a French patient
N Loux, P Benlian, D Pastier, et al.
Annales De Genetique
|
January 1, 1980
Regional assignment of catalase (CAT) gene to band 11p13. Association with the aniridia-Wilms' tumor-Gonadoblastoma (WAGR) complex
C Junien, C Turleau, J de Grouchy, et al.
Prenatal Diagnosis
|
January 1, 1981
Prenatal diagnosis of congenital enzymopenic methaemoglobinaemia with mental retardation due to generalized cytochrome b5 reductase deficiency: first report of two cases
C Junien, A Leroux, D Lostanlen, et al.
Human Genetics
|
January 1, 1980
PK3: a new chromosome enzyme marker for gene dosage studies in chromosome 15 imbalance
C Junien, H Rubinson-Skala, J C Dreyfus, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
June 8, 2001
[Hyperinsulinism]
P de Lonlay-Debeney, J C Fournet, G Touati, et al.
American Journal of Human Genetics
|
July 1, 1984
The genes coding for A alpha-, B beta-, and gamma-chains of fibrinogen map to 4q2
I Henry, G Uzan, D Weil, et al.
Page
of 29
Search research articles
Search
Showing results (181-190 of 284) with videos related to
Sort By:
Page
of 29
Annales De Medecine Interne
|
November 1, 1977
[Generalized saturnine paralysis. Discovery of a double congenital disease: glucose-6-phosphate dehydrogenase deficiency (new variant) and distal tubular acidosis]
F Nouailhat, J C Kaplan, Y Giudicelli, et al.
Human Genetics
|
July 7, 1976
Gene dosage effect in human triploid fibroblasts
C Junien, H Rubinson, J C Dreyfus, et al.
Cancer Research
|
July 1, 1995
Seven megabase yeast artificial chromosome contig at region 11p15: identification of a yeast artificial chromosome spanning the breakpoint of a chromosomal translocation found in a case of Beckwith-Wiedemann syndrome
M Negrini, S Sabbioni, M Ohta, et al.
Annales De Genetique
|
January 1, 1982
Inverted tandem duplication of the short arm of chromosome 8: a non-random de novo structural aberration in man. Localization of the gene for glutathione reductase in subband 8p21.1
P K Jensen, C Junien, S Despoisse, et al.
Human Genetics
|
July 1, 1991
Recurrent mutation at aa 792 in the LDL receptor gene in a French patient
N Loux, P Benlian, D Pastier, et al.
Annales De Genetique
|
January 1, 1980
Regional assignment of catalase (CAT) gene to band 11p13. Association with the aniridia-Wilms' tumor-Gonadoblastoma (WAGR) complex
C Junien, C Turleau, J de Grouchy, et al.
Prenatal Diagnosis
|
January 1, 1981
Prenatal diagnosis of congenital enzymopenic methaemoglobinaemia with mental retardation due to generalized cytochrome b5 reductase deficiency: first report of two cases
C Junien, A Leroux, D Lostanlen, et al.
Human Genetics
|
January 1, 1980
PK3: a new chromosome enzyme marker for gene dosage studies in chromosome 15 imbalance
C Junien, H Rubinson-Skala, J C Dreyfus, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
June 8, 2001
[Hyperinsulinism]
P de Lonlay-Debeney, J C Fournet, G Touati, et al.
American Journal of Human Genetics
|
July 1, 1984
The genes coding for A alpha-, B beta-, and gamma-chains of fibrinogen map to 4q2
I Henry, G Uzan, D Weil, et al.
Page
of 29