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Human Genetics|March 12, 1979
Ring chromosome 22 in a mentally retarded child and mosaic 45,XX,-15,-22,+t(15;22)(p11;q11)/46,XX,r(22)/46,XX karyotype in the motherJ P Fryns, H Van den Berghe
Human Genetics|September 1, 1979
Another elliptocytosis locus on chromosome 1?B J Keats
Human Genetics|September 1, 1979
Cytogenetic and clinical studies in five cases of inv dup(15)L Wisniewski, T Hassold, J Heffelfinger, et al.
Human Genetics|September 1, 1979
Concordant congenital malformations in twins with inherited translocation: t(9p--;13q+)G S Sekhon, K Taysi
Human Genetics|September 1, 1979
Cycloheximide-resistance in Chinese hamster ovary cells and human fibroblast cells. Cytogenetic and biochemical characterizationH Pöche, K H Nierhaus, S Zakrzewski
Human Genetics|September 1, 1979
Determinants of plasma uric acidC L Gulbrandsen, N E Morton, D C Rao, et al.
Human Genetics|September 2, 1979
Antenatal diagnosis of a de novo reciprocal translocation 46,XX,t(3;7)(q21;q11)P Husslein, W Schnedl, P Wagenbichler
Human Genetics|September 2, 1979
Trisomy 6p22 leads to 6pter due to familial t(6;13)(p22;q34 or 33) translocationG Rosi, G Venti, G Migliorini Brushelli, et al.
Human Genetics|May 1, 2004
An intragenic deletion/inversion event in the DMD gene determines a novel exon creation and results in a BMD phenotypeRachele Cagliani, Manuela Sironi, Emma Ciafaloni, et al.
Human Genetics|August 1, 1992
Fragile site (16) (q22). III. Segregation analysisB Müller, W Feichtinger, C Bonaïti-Pellié, et al.
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