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Results: 3

Authors: Murray, J. C. Nishimura, D. Y. Buetow, K. H. Ardinger, H. H. Spence, M. A. Sparkes, R. S. Falk, R. E. Falk, P. M. Gardner, R. J. M. Harkness, E. M. Glinski, L. P. Pauli, R. M. Nakamura, Y. Green, P. P. Schinzel, A.
Citation: C. Murray, J. et al., Linkage of an autosomal dominant clefting syndrome (van der woude) to loci on chromosome Iq, American journal of human genetics , 46-I(3), 1990, pp. 486-491

Authors: Farrar, G. J. Kenna, P. Redmond, R. McWilliam, P. Bradley, D.G. Humphries, M. M Sharp, E.M. Inglehearn, C. F. Bashir, R. Jay, M. Watty, A. Ludwig, M. Schinzel, A. Samanns, C. Gal, A. Bhattacharya, S. Humphries, P.
Citation: J. Farrar, G. et al., Autosomal dominant retinitis pigmentosa: Absence of the rhodopsin proline.histidine substitution (codon 23) in pedigrees from Europe, American journal of human genetics , 47-II(6), 1990, pp. 941-945

Authors: Biancalana, V. Briard, M. L. David, A. Gilgenkrantz, S. Kaplan, J. Mathieu, M. Piussan, C. Poncin, J. Schinzel, A. Oudet, C. Hanauer, A.
Citation: V. Biancalana, et al., Confirmation and refinement of the genetic localization of the Coffin-Lowry syndrome locus in Xp22.1-p22.2, American journal of human genetics , 50-II(5), 1992, pp. 981-987
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