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Showing results (191-200 of 461) with videos related to

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Prenatal Diagnosis|November 1, 1992
A simple electrophoretic procedure for fetal diagnosis of beta-thalassaemia due to short deletionsV Faà, M C Rosatelli, R Sardu, et al.
Journal of Medical Genetics|December 1, 1983
Phenotype-genotype correlation in haemoglobin H disease in childhoodR Galanello, M Pirastu, M A Melis, et al.
Pediatric Research|July 1, 1979
Favism in GdMediterranean heterozygous femalesG Sanna, S De Virgiliis, C Palmas, et al.
European Journal of Pediatrics|February 1, 1994
Hypothalamic growth hormone deficiency in a patient with ring chromosome 18A Meloni, L Boccone, L Angius, et al.
Genetic Testing|September 25, 1999
A strategy for fragile-X carrier screeningM A Melis, M Addis, C Lepiani, et al.
Human Mutation|January 8, 2000
A new glucose 6 phosphate dehydrogenase variant G6PD Sinnai (34 G-->T). Mutations in brief no. 156. OnlineR Galanello, D Loi, C Sollaino, et al.
Journal of Chromatography. A|October 15, 1993
Capillary electrophoresis of abnormal hemoglobins associated with alpha-thalassemiasM Zhu, T Wehr, V Levi, et al.
Hemoglobin|January 1, 1978
Hemoglobin H disease in Sardinia: phenotypic and genetic observationsR Galanello, M A Melis, M Furbetta, et al.
Blood|November 1, 1983
A family with segregating triplicated alpha globin loci and beta thalassemiaR Galanello, R Ruggeri, E Paglietti, et al.
Human Reproduction (Oxford, England)|February 1, 1994
Psychological implications and acceptability of preimplantation diagnosisM L Palomba, G Monni, R Lai, et al.
Pageof 47

Showing results (191-200 of 461) with videos related to

Sort By:
Pageof 47
Prenatal Diagnosis|November 1, 1992
A simple electrophoretic procedure for fetal diagnosis of beta-thalassaemia due to short deletionsV Faà, M C Rosatelli, R Sardu, et al.
Journal of Medical Genetics|December 1, 1983
Phenotype-genotype correlation in haemoglobin H disease in childhoodR Galanello, M Pirastu, M A Melis, et al.
Pediatric Research|July 1, 1979
Favism in GdMediterranean heterozygous femalesG Sanna, S De Virgiliis, C Palmas, et al.
European Journal of Pediatrics|February 1, 1994
Hypothalamic growth hormone deficiency in a patient with ring chromosome 18A Meloni, L Boccone, L Angius, et al.
Genetic Testing|September 25, 1999
A strategy for fragile-X carrier screeningM A Melis, M Addis, C Lepiani, et al.
Human Mutation|January 8, 2000
A new glucose 6 phosphate dehydrogenase variant G6PD Sinnai (34 G-->T). Mutations in brief no. 156. OnlineR Galanello, D Loi, C Sollaino, et al.
Journal of Chromatography. A|October 15, 1993
Capillary electrophoresis of abnormal hemoglobins associated with alpha-thalassemiasM Zhu, T Wehr, V Levi, et al.
Hemoglobin|January 1, 1978
Hemoglobin H disease in Sardinia: phenotypic and genetic observationsR Galanello, M A Melis, M Furbetta, et al.
Blood|November 1, 1983
A family with segregating triplicated alpha globin loci and beta thalassemiaR Galanello, R Ruggeri, E Paglietti, et al.
Human Reproduction (Oxford, England)|February 1, 1994
Psychological implications and acceptability of preimplantation diagnosisM L Palomba, G Monni, R Lai, et al.
Pageof 47