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Human Genetics|April 27, 1979
Partial trisomy 13 as a result of de novo (6p;13q) translocationL A Jones, K Taysi, A W Strauss, et al.
Human Genetics|June 28, 2012
The distinct and overlapping phenotypic spectra of FOXP1 and FOXP2 in cognitive disordersClaire Bacon, Gudrun A Rappold
Human Genetics|June 23, 2012
The role of phenotype in gene discovery in the whole genome sequencing eraLaura Almasy
Human Genetics|January 1, 1985
Genetic complementation of steroid sulphatase after somatic cell hybridization of X-linked ichthyosis and multiple sulphatase deficiencyA Ballabio, G Parenti, E Napolitano, et al.
Human Genetics|January 1, 1985
Direct assignment of orosomucoid to human chromosome 9 and alpha 2HS-glycoprotein to chromosome 3 using human fetal liver x rat hepatoma hybridsD W Cox, U Francke
Human Genetics|January 19, 1979
Isoelectrofocusing of erythrocyte galactose 1 phospho uridyl transferase in a family with both galactosemia and Duarte variantsF Schapira, C Gregori, J Banroques, et al.
Human Genetics|February 15, 1979
Trisomy for the distal third of the long arm of chromosome 19 in brother and sisterW Schmid
Human Genetics|March 12, 1979
The 8p- syndromeJ A Reiss, P M Brenes, J Chamberlin, et al.
Human Genetics|March 12, 1979
The length of the Y chromosome in Nubian males and its location in metaphase spreadsC E Nasjleti, C J Kowalski, J E Harris, et al.
Human Genetics|March 12, 1979
Chromosome deletion [46,XX,del(20)(q11)] in agnogenic myeloid metaplasiaL Findley, J E Kurnick, D C Peakman, et al.
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