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Cytogenetic and Genome Research|February 24, 2007
X chromosome loss and ageingL M Russell, P Strike, C E Browne, et al.Clinical Genetics|January 1, 1978
A cytogenetic survey of an institution for the mentally retarded: I. Chromosome abnormalitiesP A Jacobs, J S Matsuura, M Mayer, et al.American Journal of Human Genetics|July 1, 1979
Late replicating X chromosomes in human triploidyP A Jacobs, A M Matsuyama, I M Buchanan, et al.Human Genetics|September 12, 2000
Seven ring (X) chromosomes lacking the XIST locus, six with an unexpectedly mild phenotypeC Turner, N R Dennis, D H Skuse, et al.American Journal of Medical Genetics|June 1, 1982
Marker X syndrome in an oriental family with probable transmission by a normal maleF A Rhoads, A C Oglesby, M Mayer, et al.Human Genetics|January 1, 1985
A cytogenetic study of a population of retarded females with special reference to the fragile (X) syndromeM Mayer, M A Abruzzo, P A Jacobs, et al.Journal of Medical Genetics|February 1, 1992
Estimates of the frequency of chromosome abnormalities detectable in unselected newborns using moderate levels of bandingP A Jacobs, C Browne, N Gregson, et al.Annals of Human Genetics|January 1, 1984
The marker (X) syndrome: a cytogenetic and genetic analysisS L Sherman, N E Morton, P A Jacobs, et al.Birth Defects Original Article Series|January 1, 1990
The parental origin of the missing or additional chromosome in 45,X and 47,XXX femalesT Hassold, K Arnovitz, P A Jacobs, et al.Human Molecular Genetics|March 1, 1994
Insert size and flanking haplotype in fragile X and normal populations: possible multiple origins for the fragile X mutationJ N Macpherson, H Bullman, S A Youings, et al.Pageof 17