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Showing results 1 to 6 of 6

	Title	Author(s)	Issue Date
	Assignment of the human homolog of mouse Dlx3 to Chromosome 17q21.3-q22 by analysis of somatic cell hybrids and fluorescence in situ hybridization Journal:Mammalian Genome	Scherer, SW Heng, HHQ Robinson, GW Mahon, KA Evans, JP Tsui, LC	1995
	Characterization of the split hand/split foot malformation locus SHFM1 at 7q21.3-q22.1 and analysis of a candidate gene for its expression during limb development Journal:Human Molecular Genetics	Crackower, MA Scherer, SW Rommens, JM Hui, CC Poorkaj, P Soder, S Cobben, JM Hudgins, L Evans, JP Tsui, LC	1996
	Evidence for locus heterogeneity in human autosomal dominant split hand/split foot malformation Journal:American Journal of Human Genetics	Palmer, SE Scherer, SW Kukolich, M Wijsman, EM Tsui, LC Stephens, K Evans, JP	1994
	Fine mapping of the autosomal dominant split hand/split foot locus on chromosome 7, band q21.3-q22.1	Scherer, SW Poorkaj, P Allen, T Kim, J Geshuri, D Nunes, M Soder, S Stephens, K Pagon, RA Patton, MA Berg, MA Donlon, T Rivera, H Pfeiffer, RA Naritomi, K Hughes, H Genuardi, M Gurrieri, F Neri, G Lovrein, E Magenis, E Tsui, L-C Evans, JP	1994
	Heterogeneity of the autosomal dominant split hand/split foot malformation [6] Journal:American Journal of Human Genetics	Zlotogora, J Evans, JP Palmer, S Scherer, SW Kukolich, M Wijsman, EM Tsui, LC Stephens, K	1995
	Physical mapping of the split hand/split foot locus on chromosome 7 and implication in syndromic ectrodactyly Journal:Human Molecular Genetics	Scherer, SW Poorkaj, P Massa, H Soder, S Allen, T Nunes, M Geshuri, D Wong, E Belloni, E Little, S Zhou, L Becker, D Kere, J Ignatius, J Niikawa, N Fukushima, Y Hasegawa, T Weissenbach, J Boncinelli, E Trask, B Tsui, L-C Evans, JP	1994

Showing results 1 to 6 of 6