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Human Genetics|April 1, 1989
Parental age and the origin of trisomy 21. A study of 302 familiesF Dagna Bricarelli, M Pierluigi, M Landucci, et al.Cancer Research|December 1, 1986
Terminal erythroid differentiation in the K-562 cell line by 1-beta-D-arabinofuranosylcytosine: accompaniment by c-myc messenger RNA decreaseG L Bianchi Scarrà, M Romani, D A Coviello, et al.Human Genetics|January 1, 1981
Expression of GALT in two unrelated 9p- patients. Evidence for assignment of the GALT locus to the 9p21 bandF Dagna Bricarelli, M Magnani, A Arslanian, et al.International Journal of Andrology|May 30, 2012
Clinical correlates of sex steroids and gonadotropins in men over the late adulthood: the Framingham Heart StudyR Haring, V Xanthakis, A Coviello, et al.Growth Hormone & IGF Research : Official Journal of the Growth Hormone Research Society and the International IGF Research Society|October 11, 2005
Heterozygous mutations of growth hormone receptor gene in children with idiopathic short statureEugenio Bonioli, Marina Tarò, Carmen La Rosa, et al.Cancer Research|March 1, 1994
Estradiol inhibits growth of hormone-nonresponsive PC3 human prostate cancer cellsG Carruba, U Pfeffer, E Fecarotta, et al.Biochemical and Molecular Medicine|February 12, 1998
Phenotypic comparison of an osteogenesis imperfecta type IV proband with a de novo alpha2(I) Gly922 --> Ser substitution in type I collagen and an unrelated patient with an identical mutationA Forlino, E D'amato, M Valli, et al.Journal of Pediatric Gastroenterology and Nutrition|December 2, 2010
Clinical features and genotype-phenotype correlations in children with progressive familial intrahepatic cholestasis type 3 related to ABCB4 mutationsCarla Colombo, Pietro Vajro, Dario Degiorgio, et al.American Journal of Human Genetics|July 1, 1992
A large deletion in the LDL receptor gene--the cause of familial hypercholesterolemia in three Italian families: a study that dates back to the 17th century (FH-Pavia)S Bertolini, N Lelli, D A Coviello, et al.Gene|October 19, 2022
Identification of alternative transcripts of NSD1 gene in Sotos Syndrome patients and healthy subjectsGiuseppina Conteduca, Barbara Testa, Chiara Baldo, et al.Pageof 13