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Human Mutation
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January 1, 1996
A missense (T577I) mutation in the luteinizing hormone receptor gene associated with familial male-limited precocious puberty
S Cocco, A Meloni, M G Marini, et al.
Pediatric Research
|
February 1, 1984
Longitudinal study of a newborn with a combination of deletion and nondeletion alpha-thalassemia-2
R Galanello, M A Melis, L Maccioni, et al.
American Journal of Medical Genetics
|
July 1, 1994
Blepharophimosis, ptosis, epicanthus inversus syndrome, a new case associated with de novo balanced autosomal translocation [46,XY,t(3;7)(q23;q32)]
L Boccone, A Meloni, A M Falchi, et al.
Eye (London, England)
|
March 29, 2024
Correction: Retinal non-perfusion: recognizing and defining what is important
Jessica A Cao, Hasenin Al-Khersan, Varun Chaudhary, et al.
Sheng Wu Gong Cheng Xue Bao = Chinese Journal of Biotechnology
|
November 13, 2001
[The chemical decomposition of glutamine and its effect on hybridoma cell culture]
Y Xin, Y Yang, Q Li, et al.
Journal of Medical Genetics
|
February 1, 1981
Interaction of alpha- and delta beta o- thalassaemia: haematological features and globin chain synthesis analysis
R Galanello, M Furbetta, M A Melis, et al.
Journal of Clinical Ultrasound : JCU
|
March 1, 1995
Color Doppler ultrasound and prenatal diagnosis of cleft palate
G Monni, R M Ibba, G Olla, et al.
American Journal of Obstetrics and Gynecology
|
April 1, 1987
Chorionic villus sampling by rigid forceps: experience with 300 cases at risk for thalassemia major
G Monni, R M Ibba, G Olla, et al.
Prenatal Diagnosis
|
July 1, 1988
Prenatal diagnosis of beta-thalassaemia by second-trimester chorionic villus sampling
G Monni, R M Ibba, G Olla, et al.
Progress in Clinical and Biological Research
|
January 1, 1989
Interaction between deletion delta-thalassemia and beta zero-thalassemia (codon 39 nonsense mutation) in a Sardinian family
R Galanello, A Podda, M A Melis, et al.
Page
of 47
Search research articles
Search
Showing results (131-140 of 461) with videos related to
Sort By:
Page
of 47
Human Mutation
|
January 1, 1996
A missense (T577I) mutation in the luteinizing hormone receptor gene associated with familial male-limited precocious puberty
S Cocco, A Meloni, M G Marini, et al.
Pediatric Research
|
February 1, 1984
Longitudinal study of a newborn with a combination of deletion and nondeletion alpha-thalassemia-2
R Galanello, M A Melis, L Maccioni, et al.
American Journal of Medical Genetics
|
July 1, 1994
Blepharophimosis, ptosis, epicanthus inversus syndrome, a new case associated with de novo balanced autosomal translocation [46,XY,t(3;7)(q23;q32)]
L Boccone, A Meloni, A M Falchi, et al.
Eye (London, England)
|
March 29, 2024
Correction: Retinal non-perfusion: recognizing and defining what is important
Jessica A Cao, Hasenin Al-Khersan, Varun Chaudhary, et al.
Sheng Wu Gong Cheng Xue Bao = Chinese Journal of Biotechnology
|
November 13, 2001
[The chemical decomposition of glutamine and its effect on hybridoma cell culture]
Y Xin, Y Yang, Q Li, et al.
Journal of Medical Genetics
|
February 1, 1981
Interaction of alpha- and delta beta o- thalassaemia: haematological features and globin chain synthesis analysis
R Galanello, M Furbetta, M A Melis, et al.
Journal of Clinical Ultrasound : JCU
|
March 1, 1995
Color Doppler ultrasound and prenatal diagnosis of cleft palate
G Monni, R M Ibba, G Olla, et al.
American Journal of Obstetrics and Gynecology
|
April 1, 1987
Chorionic villus sampling by rigid forceps: experience with 300 cases at risk for thalassemia major
G Monni, R M Ibba, G Olla, et al.
Prenatal Diagnosis
|
July 1, 1988
Prenatal diagnosis of beta-thalassaemia by second-trimester chorionic villus sampling
G Monni, R M Ibba, G Olla, et al.
Progress in Clinical and Biological Research
|
January 1, 1989
Interaction between deletion delta-thalassemia and beta zero-thalassemia (codon 39 nonsense mutation) in a Sardinian family
R Galanello, A Podda, M A Melis, et al.
Page
of 47