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Human Genetics|May 1, 1996
A new point mutation affecting the fourth transmembrane domain of PMP22 results in severe de novo Charcot-Marie-Tooth diseaseR Navon, B Seifried, N S Gal-On, et al.Human Genetics|May 1, 1996
A new XmnI polymorphism in the regulatory region of the corticotropin releasing hormone geneC G Baerwald, G S Panayi, J S LanchburyHuman Genetics|March 12, 1979
PEP A9, a new, unstable variant in the peptidase A systemP Kühnl, K Anneken, W SpielmannHuman Genetics|November 1, 1995
Susceptibility of heterochromatin to aphidicolin-induced chromosomal breakageA M Dominguez, S A Smith, I F GreenbaumHuman Genetics|November 1, 1995
Complement component C3: molecular basis of the C3*S025 variant and evidence for molecular heterogeneity of other variantsT Höhler, M Botto, C Rittner, et al.Human Genetics|November 1, 1995
Influence of transcription and replication on the in situ resolution of immunoglobulin heavy-chain constant region genes: an interphase cytogenetics analysisM Telhada, C Carvalho, M Carmo-Fonseca, et al.Human Genetics|November 1, 1995
A sublocus of the multicopy microsatellite marker CMS1 maps proximal to spinal muscular atrophy (SMA) as shown by recombinant analysisG van der Steege, J M Cobben, J Osinga, et al.Human Genetics|December 1, 1995
Detection of chromosome aberrations in paraffin sections of seven gonadal yolk sac tumors of childhoodJ Jenderny, E Köster, A Meyer, et al.Human Genetics|December 1, 1995
Parental generalized EEG alpha activity predisposes to spike wave discharges in offspringH Doose, E Castiglione, S WaltzHuman Genetics|December 1, 1995
APC mutation in the alternatively spliced region of exon 9 associated with late onset familial adenomatous polyposisR B van der Luijt, H F Vasen, C M Tops, et al.Pageof 959