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Nature|January 3, 1991
Localization of the X inactivation centre on the human X chromosome in Xq13C J Brown, R G Lafreniere, V E Powers, et al.
American Journal of Human Genetics|January 1, 1989
Fine structure DNA mapping studies of the chromosomal region harboring the genetic defect in neurofibromatosis type IP O'Connell, R J Leach, D H Ledbetter, et al.
American Journal of Human Genetics|February 1, 1988
Uniparental disomy as a mechanism for human genetic diseaseJ E Spence, R G Perciaccante, G M Greig, et al.
Genomics|May 23, 1998
The human ROX gene: genomic structure and mutation analysis in human breast tumorsC Lo Nigro, T Venesio, A Reymond, et al.
Clinical Genetics|June 14, 2000
Somatic segregation errors predominantly contribute to the gain or loss of a paternal chromosome leading to uniparental disomy for chromosome 15W P Robinson, S L Christian, B D Kuchinka, et al.
Genome Research|March 21, 1998
Integrated YAC contig map of the Prader-Willi/Angelman region on chromosome 15q11-q13 with average STS spacing of 35 kbS L Christian, N K Bhatt, S A Martin, et al.
American Journal of Diseases of Children (1960)|May 1, 1985
Survival of infants with spina bifida--Atlanta, 1972-1979M M Adams, F Greenberg, M J Khoury, et al.
American Journal of Epidemiology|January 1, 1996
Hispanic origin and neural tube defects in Houston/Harris County, Texas. I. Descriptive epidemiologyM A Canfield, J F Annegers, J D Brender, et al.
Pediatrics|May 1, 1983
A population study of the VACTERL association: evidence for its etiologic heterogeneityM J Khoury, J F Cordero, F Greenberg, et al.
Human Molecular Genetics|July 1, 1995
A gene for a severe lethal form of X-linked arthrogryposis (X-linked infantile spinal muscular atrophy) maps to human chromosome Xp11.3-q11.2H Kobayashi, L Baumbach, T C Matise, et al.
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