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American Journal of Human Genetics|September 25, 2003
Myotonic dystrophy type 2: human founder haplotype and evolutionary conservation of the repeat tractChristina L Liquori, Yoshio Ikeda, Marcy Weatherspoon, et al.
American Journal of Human Genetics|October 15, 2003
A major susceptibility locus on chromosome 22q12 plays a critical role in the control of kala-azarBruno Bucheton, Laurent Abel, Sayda El-Safi, et al.
American Journal of Human Genetics|October 1, 1992
Molecular analysis of mutations in a patient with purine nucleoside phosphorylase deficiencyM R Aust, L G Andrews, M J Barrett, et al.
American Journal of Human Genetics|November 1, 1992
A molecular deletion of distal chromosome 4p in two families with a satellited chromosome 4 lacking the Wolf-Hirschhorn syndrome phenotypeL L Estabrooks, A N Lamb, H N Kirkman, et al.
American Journal of Human Genetics|March 1, 1992
The meiotic stage of nondisjunction in trisomy 21: determination by using DNA polymorphismsS E Antonarakis, M B Petersen, M G McInnis, et al.
American Journal of Human Genetics|March 1, 1992
Involvement of multiple chromosome 17p loci in medulloblastoma tumorigenesisP H Cogen, L Daneshvar, A K Metzger, et al.
American Journal of Human Genetics|April 1, 1992
PCR amplification of alleles at the DIS80 locus: comparison of a Finnish and a North American Caucasian population sample, and forensic casework evaluationA Sajantila, B Budowle, M Ström, et al.
American Journal of Human Genetics|January 1, 1992
Identification of novel RFLPs in the vicinity of CpG islands in Xq28: application to the analysis of the pattern of X chromosome inactivationE Maestrini, S Rivella, C Tribioli, et al.
American Journal of Human Genetics|June 1, 1992
Correction of sulfatide metabolism after transfer of prosaposin cDNA to cultured cells from a patient with SAP-1 deficiencyM A Rafi, S Amini, X L Zhang, et al.
American Journal of Human Genetics|June 6, 2003
Loss of kindlin-1, a human homolog of the Caenorhabditis elegans actin-extracellular-matrix linker protein UNC-112, causes Kindler syndromeDawn H Siegel, Gabrielle H S Ashton, Homero G Penagos, et al.
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