Showing results (451-460 of 6,483) with videos related to
Sort By:
Pageof 649
Journal of Medical Genetics|June 1, 1988
Birth defects following maternal exposure to ergotamine, beta blockers, and caffeineH E Hughes, D A GoldsteinJournal of Medical Genetics|June 1, 1988
New autosomal recessive faciodigitogenital syndromeA S Teebi, K K Naguib, S Al-Awadi, et al.Journal of Medical Genetics|June 1, 1988
Oculotrichodysplasia (OTD): a new probably autosomal recessive conditionL Cecatto-De-Lima, M Pinheiro, N Freire-MaiaJournal of Medical Genetics|August 5, 2021
Homozygous mutations in CCDC34 cause male infertility with oligoasthenoteratozoospermia in humans and miceJiangshan Cong, Xiong Wang, Amir Amiri-Yekta, et al.Journal of Medical Genetics|August 5, 2021
Revisiting the UK Genetic Severity Score for NF2: a proposal for the addition of a functional genetic componentNúria Catasús, Belen Garcia, Iván Galván-Femenía, et al.Journal of Medical Genetics|June 3, 2020
Genotype-phenotype correlations for pancreatic cancer risk in Dutch melanoma families with pathogenic CDKN2A variantsKasper A Overbeek, Mar Dm Rodríguez-Girondo, Anja Wagner, et al.Journal of Medical Genetics|October 1, 1987
Association of tetra-amelia, ectodermal dysplasia, hypoplastic lacrimal ducts and sacs opening towards the exterior, peculiar face, and developmental retardationS Ohdo, H Madokoro, T Sonoda, et al.Journal of Medical Genetics|October 1, 1987
Hydatidiform mole: parental chromosome aberrations in partial and complete molesL O Vejerslev, R A Fisher, U Surti, et al.Journal of Medical Genetics|October 1, 1987
Brachmann-de Lange syndrome in sibsK K Naguib, A S Teebi, S A Al-Awadi, et al.Journal of Medical Genetics|June 3, 1999
Germline mutations of the LKB1 (STK11) gene in Peutz-Jeghers patientsZ J Wang, M Churchman, E Avizienyte, et al.Pageof 649