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NARA Subscribed7
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Springer Nature7
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Human Genetics6
Immunogenetics1
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20071
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19972
Gerd Utermann results 7 · Newest (Page 1/1, per page 25)
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Tracing genetic history of modern humans using X-chromosome lineagesNARA Subscribed
Human Genetics · 2007 · Vol. 122 · Issue 5 · Springer
Vania Yotova; Jean-François Lefebvre; Oleksiy Kohany; Jerzy Jurka; Roman Michalski; David Modiano; Gerd Utermann; Scott M. Williams; Damian Labuda
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Progressive hearing loss, and recurrent sudden sensorineural hearing loss associated with GJB2 mutations – phenotypic spectrum and frequencies of GJB2 mutations in AustriaNARA Subscribed
Human Genetics · 2002 · Vol. 111 · Issue 2 · Springer
Andreas R. Janecke; Almut Hirst-Stadlmann; Barbara Günther; Barbara Utermann; Thomas Müller; Judith Löffler; Gerd Utermann; Doris Nekahm-Heis
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High-resolution mapping of the human 4q21 and the mouse 5E3 SCYB chemokine cluster by fiber-fluorescence in situ hybridizationNARA Subscribed
Immunogenetics · 2001 · Vol. 53 · Issue 7 · Springer
Martin Erdel; Milan Theurl; Martina Meyer; Hans-Christoph Duba; Gerd Utermann; Gabriele Werner-Felmayer
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De novo mutation of the connexin 26 gene associated with dominant non-syndromic sensorineural hearing lossNARA Subscribed
Human Genetics · 2001 · Vol. 108 · Issue 3 · Springer
Andreas R Janecke; Doris Nekahm; Judith Löffler; Almut Hirst-Stadlmann; Thomas Müller; Gerd Utermann
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Mutation analysis in glycogen storage disease type 1 non-aNARA Subscribed
Human Genetics · 2000 · Vol. 107 · Issue 3 · Springer
Andreas R. Janecke; Martin Lindner; Martin Erdel; Ertan Mayatepek; Dorothea Möslinger; Teodor Podskarbi; Friedrich Fresser; Silvia Stöckler-Ipsiroglu; Georg F. Hoffmann; Gerd Utermann
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Chromosomal instability in a woman with infertility and two unaffected brothers: a new familial chromosomal breakage syndrome?NARA Subscribed
Human Genetics · 1997 · Vol. 100 · Issue 3-4 · Springer
H.-C. Duba; Harald G. Weirich; Helga Weirich-Schwaiger; Barbara Utermann; David Nachbaur; Elisabeth Sölder; Gerd Utermann
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Comparative genomic hybridization reveals a partial de novo trisomy 6q23-qter in an infant with congenital malformations: delineation of the phenotypeNARA Subscribed
Human Genetics · 1997 · Vol. 99 · Issue 5 · Springer
M. Erdel; Hans-Christoph Duba; Irmgard Verdorfer; Arno Lingenhel; Ralf Geiger; Karl-Heinz Gutenberger; Edgar Ludescher; Barbara Utermann; Gerd Utermann
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