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Cytogenetics and Cell Genetics|January 1, 1995
A region-specific microdissection library for human chromosome 2p23-->p21 and the analysis of an interstitial deletion of 2p21F T Kao, J Yu, J Qi, et al.
American Journal of Medical Genetics|September 19, 1997
Clinical and molecular analysis in Joubert syndromeJ E Pellegrino, M W Lensch, M Muenke, et al.
Cytogenetics and Cell Genetics|August 31, 2000
The genomic structure, chromosome location, and analysis of the human DKK1 head inducer gene as a candidate for holoprosencephalyE Roessler, Y Du, A Glinka, et al.
American Journal of Medical Genetics|August 3, 2001
Novel SNP at the common primer site of exon IIIa of FGFR2 gene causes error in molecular diagnosis of craniosynostosis syndromeL J Wong, T J Chen, P Dai, et al.
Genomics|January 1, 1996
Human enteric defensin genes: chromosomal map position and a model for possible evolutionary relationshipsC L Bevins, D E Jones, A Dutra, et al.
Cytogenetic and Genome Research|November 20, 2002
The genomic structure, chromosomal localization, and analysis of SIL as a candidate gene for holoprosencephalyJ D Karkera, S Izraeli, E Roessler, et al.
American Journal of Medical Genetics|October 23, 1997
Genomic structure, sequence, and mapping of human FGF8 with no evidence for its role in craniosynostosis/limb defect syndromesK Yoshiura, N J Leysens, J Chang, et al.
Genomics|October 1, 1990
Partial deletions of a sequence family ("DXS278") and its physical linkage to steroid sulfatase as detected by pulsed-field gel electrophoresisR E Schnur, R G Knowlton, M A Musarella, et al.
The Journal of Bone and Joint Surgery. American Volume|August 1, 1993
Genetic transmission of fibrodysplasia ossificans progressiva. Report of a familyF S Kaplan, W McCluskey, G Hahn, et al.
American Journal of Human Genetics|November 1, 1995
Physical mapping of the holoprosencephaly critical region in 18p11.3J Overhauser, H F Mitchell, E H Zackai, et al.
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