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A Cao

Showing results (131-140 of 461) with videos related to

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Human Mutation|January 1, 1996
A missense (T577I) mutation in the luteinizing hormone receptor gene associated with familial male-limited precocious pubertyS 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-2R 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 importantJessica 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 analysisR Galanello, M Furbetta, M A Melis, et al.
Journal of Clinical Ultrasound : JCU|March 1, 1995
Color Doppler ultrasound and prenatal diagnosis of cleft palateG 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 majorG Monni, R M Ibba, G Olla, et al.
Prenatal Diagnosis|July 1, 1988
Prenatal diagnosis of beta-thalassaemia by second-trimester chorionic villus samplingG 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 familyR Galanello, A Podda, M A Melis, et al.
Pageof 47

Showing results (131-140 of 461) with videos related to

Sort By:
Pageof 47
Human Mutation|January 1, 1996
A missense (T577I) mutation in the luteinizing hormone receptor gene associated with familial male-limited precocious pubertyS 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-2R 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 importantJessica 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 analysisR Galanello, M Furbetta, M A Melis, et al.
Journal of Clinical Ultrasound : JCU|March 1, 1995
Color Doppler ultrasound and prenatal diagnosis of cleft palateG 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 majorG Monni, R M Ibba, G Olla, et al.
Prenatal Diagnosis|July 1, 1988
Prenatal diagnosis of beta-thalassaemia by second-trimester chorionic villus samplingG 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 familyR Galanello, A Podda, M A Melis, et al.
Pageof 47