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Human Genetics|October 1, 1988
Retinal/macular pigmentation in conjunction with ring 14 chromosomeP J Howard, D Clark, J DearloveHuman Genetics|October 1, 1988
A frequent factor XII gene mutation in Hageman traitF Bernardi, G Marchetti, S Volinia, et al.Human Genetics|October 1, 1988
Siblings with chromosome mosaicism, microcephaly, and growth retardation: the phenotypic expression of a human mitotic mutant?J L Tolmie, E Boyd, P Batstone, et al.Human Genetics|November 9, 2019
Considerations for whole exome sequencing unique to prenatal careAhmad Abou Tayoun, Heather Mason-SuaresHuman Genetics|May 19, 2022
Homozygous missense mutation in CCDC155 disrupts the transmembrane distribution of CCDC155 and SUN1, resulting in non-obstructive azoospermia and premature ovarian insufficiency in humansHuan Wu, Xin Zhang, Rong Hua, et al.Human Genetics|September 1, 1988
Tight linkage between myotonic dystrophy and apolipoprotein E genes revealed with allele-specific oligonucleotidesB Smeets, J Poddighe, H Brunner, et al.Human Genetics|September 1, 1988
Myopia and intelligence: a pleiotropic relationship?S J Cohn, C M Cohn, A R JensenHuman Genetics|September 1, 1988
Mapping of the Emery-Dreifuss gene through reconstruction of crossover points in two Italian pedigreesG Romeo, L Roncuzzi, S Sangiorgi, et al.Human Genetics|September 1, 1988
Xp21 DNA microdeletion in a patient with chronic granulomatous disease, retinitis pigmentosa, and McLeod phenotypeG de Saint-Basile, M C Bohler, A Fischer, et al.Human Genetics|September 1, 1988
Beta-globin gene linked DNA haplotypes and frameworks in three South-East Asian populationsJ Hundrieser, T Sanguansermsri, T Papp, et al.Pageof 957