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Anales Espanoles De Pediatria
|
April 1, 1992
[Importance of molecular diagnosis in the detection of healthy male transmitters of the fragile X syndrome]
E Tizzano Ferrari, P Gallano Petit, M Baiget Bastus
Acta Haematologica
|
January 1, 1976
Haemoglobin Lepore Boston in a Spanish family
E Gimferrer, M Baiget, P D Darbre, et al.
Human Molecular Genetics
|
June 1, 1997
Somatic instability of the myotonic dystrophy (CTG)n repeat during human fetal development
L Martorell, K Johnson, C A Boucher, et al.
Sangre
|
February 1, 1991
[Hemoglobin F Catalonia. A new variant of fetal hemoglobin]
L Font, M Baiget, E Contreras, et al.
Neurologia (Barcelona, Spain)
|
March 1, 1990
[Genetic analysis of Spanish families with myotonic dystrophy]
A M Cobo, J M Martínez, J Pradas, et al.
Medicina Clinica
|
November 24, 1984
[Cooley's anemia syndrome in a double heterozygote for hemoglobin Lepore Washington-Boston and beta thalassemia]
J J Ortega, M Baiget, C Aulesa, et al.
Human Genetics
|
October 1, 1991
3' creatine kinase (M-type) polymorphisms linked to myotonic dystrophy in Italian and Spanish populations
M Gennarelli, G Novelli, A Cobo, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
April 7, 2005
Utility of a (GT) dinucleotide repeat in intron 1 of the factor 8 gene for haemophilia A carrier diagnosis
E Tizzano, A Venceslá, M Cornet, et al.
Journal of Medical Genetics
|
December 1, 1994
Meiotic drive at the myotonic dystrophy locus
M Gennarelli, B Dallapiccola, M Baiget, et al.
Leukemia Research
|
June 22, 1999
Prevalence of hemochromatosis related HFE gene mutations in patients with acute myeloid leukemia
E Gimferrer, J Nomdedeu, I Gich, et al.
Page
of 22
Search research articles
Search
Showing results (41-50 of 217) with videos related to
Sort By:
Page
of 22
Anales Espanoles De Pediatria
|
April 1, 1992
[Importance of molecular diagnosis in the detection of healthy male transmitters of the fragile X syndrome]
E Tizzano Ferrari, P Gallano Petit, M Baiget Bastus
Acta Haematologica
|
January 1, 1976
Haemoglobin Lepore Boston in a Spanish family
E Gimferrer, M Baiget, P D Darbre, et al.
Human Molecular Genetics
|
June 1, 1997
Somatic instability of the myotonic dystrophy (CTG)n repeat during human fetal development
L Martorell, K Johnson, C A Boucher, et al.
Sangre
|
February 1, 1991
[Hemoglobin F Catalonia. A new variant of fetal hemoglobin]
L Font, M Baiget, E Contreras, et al.
Neurologia (Barcelona, Spain)
|
March 1, 1990
[Genetic analysis of Spanish families with myotonic dystrophy]
A M Cobo, J M Martínez, J Pradas, et al.
Medicina Clinica
|
November 24, 1984
[Cooley's anemia syndrome in a double heterozygote for hemoglobin Lepore Washington-Boston and beta thalassemia]
J J Ortega, M Baiget, C Aulesa, et al.
Human Genetics
|
October 1, 1991
3' creatine kinase (M-type) polymorphisms linked to myotonic dystrophy in Italian and Spanish populations
M Gennarelli, G Novelli, A Cobo, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
April 7, 2005
Utility of a (GT) dinucleotide repeat in intron 1 of the factor 8 gene for haemophilia A carrier diagnosis
E Tizzano, A Venceslá, M Cornet, et al.
Journal of Medical Genetics
|
December 1, 1994
Meiotic drive at the myotonic dystrophy locus
M Gennarelli, B Dallapiccola, M Baiget, et al.
Leukemia Research
|
June 22, 1999
Prevalence of hemochromatosis related HFE gene mutations in patients with acute myeloid leukemia
E Gimferrer, J Nomdedeu, I Gich, et al.
Page
of 22