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Human Genetics|November 14, 2009
Linkage and sequence analysis indicate that CCBE1 is mutated in recessively inherited generalised lymphatic dysplasiaFiona Connell, Kamini Kalidas, Pia Ostergaard, et al.Human Genetics|November 4, 2009
The transcription factor GATA-2 does not associate with angiographic coronary artery disease in the Ottawa Heart Genomics and Cleveland Clinic GeneBank StudiesSonny Dandona, Li Chen, Meng Fan, et al.Human Genetics|January 1, 1988
Fragile sites induced by FUdR, caffeine, and aphidicolin. Their frequency, distribution, and analysisP N Rao, N A Heerema, C G PalmerHuman Genetics|January 1, 1988
Genetics of the quantitative Lp(a) lipoprotein trait. I. Relation of LP(a) glycoprotein phenotypes to Lp(a) lipoprotein concentrations in plasmaG Utermann, H G Kraft, H J Menzel, et al.Human Genetics|January 1, 1988
Chromosomal radiosensitivity of Down syndrome lymphocytes at different stages of the cell cycleH M Shafik, W W Au, M S LegatorHuman Genetics|December 1, 1987
Issues in analysis of data on paternal age and 47,+21: implications for genetic counseling for Down syndromeE B HookHuman Genetics|April 26, 2018
Loss of function mutations in VARS encoding cytoplasmic valyl-tRNA synthetase cause microcephaly, seizures, and progressive cerebral atrophyJoshi Stephen, Sheela Nampoothiri, Aditi Banerjee, et al.Human Genetics|January 1, 1985
A mitotic recombination in Wilms tumor occurs between the parathyroid hormone locus and 11p13A M Raizis, D M Becroft, R L Shaw, et al.Human Genetics|January 1, 1985
Molecular analysis of gene deletion in aniridia--Wilms tumor associationE E Michalopoulos, P J Bevilacqua, N Stokoe, et al.Human Genetics|January 1, 1985
DNA polymorphism in the 5' flanking region of the human carbonic anhydrase II gene on chromosome 8B L Lee, P J Venta, R E TashianPageof 958