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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.Medical Image Analysis|March 6, 2007
An atlas-based method to compensate for brain shift: preliminary resultsPrashanth Dumpuri, Reid C Thompson, Benoit M Dawant, et al.Journal of Perinatal Medicine|January 1, 1991
Early antenatal sonographic diagnosis of conjoined syncephalus-craniothoraco-omphalopagus twins. Case reportG Monni, C Useli, R M Ibba, et al.Archives of Ophthalmology (Chicago, Ill. : 1960)|April 1, 1996
Deletion in the peripherin/RDS gene in two unrelated Sardinian families with autosomal dominant butterfly-shaped macular dystrophyM Fossarello, C Bertini, M S Galantuomo, et al.Pageof 37