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American Journal of Human Genetics|September 16, 1999
A generalization of the transmission/disequilibrium test for uncertain-haplotype transmissionD Clayton
American Journal of Human Genetics|June 12, 1999
X-linked dyskeratosis congenita is predominantly caused by missense mutations in the DKC1 geneS W Knight, N S Heiss, T J Vulliamy, et al.
American Journal of Human Genetics|June 12, 1999
MEFV-Gene analysis in armenian patients with Familial Mediterranean fever: diagnostic value and unfavorable renal prognosis of the M694V homozygous genotype-genetic and therapeutic implicationsC Cazeneuve, T Sarkisian, C Pêcheux, et al.
American Journal of Human Genetics|June 12, 1999
Noninvasive test for fragile X syndrome, using hair root analysisR Willemsen, B Anar, Y De Diego Otero, et al.
American Journal of Human Genetics|June 12, 1999
Campomelic dysplasia translocation breakpoints are scattered over 1 Mb proximal to SOX9: evidence for an extended control regionD Pfeifer, R Kist, K Dewar, et al.
American Journal of Human Genetics|June 12, 1999
In Swedish families with hereditary prostate cancer, linkage to the HPC1 locus on chromosome 1q24-25 is restricted to families with early-onset prostate cancerH Grönberg, J Smith, M Emanuelsson, et al.
American Journal of Human Genetics|June 12, 1999
Osteoarthritis-susceptibility locus on chromosome 11q, detected by linkageK Chapman, Z Mustafa, C Irven, et al.
American Journal of Human Genetics|June 12, 1999
A test of transmission/disequilibrium for quantitative traits in pedigree data, by multiple regressionV George, H K Tiwari, X Zhu, et al.
American Journal of Human Genetics|October 16, 1999
The A1555G mutation in the 12S rRNA gene of human mtDNA: recurrent origins and founder events in families affected by sensorineural deafnessA Torroni, F Cruciani, C Rengo, et al.
American Journal of Human Genetics|October 16, 1999
Methylation imprinting of H19 and SNRPN genes in human benign ovarian teratomasK Miura, M Obama, K Yun, et al.
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