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