Familial skewed X inactivation : A molecular trait associated with high spontaneous-abortion rate maps to Xq28PEGORARO, E; WHITAKER, J; MOWERY-RUSHTON, P et al.American journal of human genetics. 1997, Vol 61, Num 1, pp 160-170, issn 0002-9297Article

DNA methylation patterns in human tissues of uniparental origin using a zinc-finger gene (ZNF127) from the Angelman/Prader-Willi regionMOWERY-RUSHTON, P. A; DRISCOLL, D. J; NICHOLLS, R. D et al.American journal of medical genetics. 1996, Vol 61, Num 2, pp 140-146, issn 0148-7299Article

Molecular cytogenetics : An essential component of modern prenatal diagnosis. DiscussionHOGGRE, W. A; SURTI, U; KOCHMAR, S. J et al.American journal of obstetrics and gynecology. 1996, Vol 175, Num 2, pp 352-357, issn 0002-9378Conference Paper

Pitt-Rogers-Danks syndrome : The result of a 4p microdeletionCLEMENS, M; MARTSOLF, J. T; ROGERS, J. G et al.American journal of medical genetics. 1996, Vol 66, Num 1, pp 95-100, issn 0148-7299Article

Efficient transfer and sustained high expression of the human glugococerebrosidase gene in mice and their functional macrophages following transplantation of bone marrow transduced by a retroviral vectorOHASHI, T; BOGGS, S; CLARK, S et al.Proceedings of the National Academy of Sciences of the United States of America. 1992, Vol 89, Num 23, pp 11332-11336, issn 0027-8424Article

The use of interphase FISH for prenatal diagnosis of Pallister-Killian syndromeMOWERY-RUSHTON, P. A; STADLER, M. P; KOCHMAR, S. J et al.Prenatal diagnosis. 1997, Vol 17, Num 3, pp 255-265, issn 0197-3851Article

Identification of mosaicism in Prader-Willi syndrome using fluorescent in situ hybridizationMOWERY-RUSHTON, P. A; HANCHETT, J. M; ZIPF, W. B et al.American journal of medical genetics. 1996, Vol 66, Num 4, pp 403-412, issn 0148-7299Article

Newborn infant with inherited ring and de novo interstitial deletion on homologous chromosome 22sWENGER, S. L; BOONE, L. Y; CUMMINS, J. H et al.American journal of medical genetics. 2000, Vol 91, Num 5, pp 351-354, issn 0148-7299Article

Identification of an unbalanced cryptic translocation t(9;17)(q34.3;p13.3) in a child with dysmorphic featuresESTOP, A. M; MOWERY-RUSHTON, P. A; CIEPLY, K. M et al.Journal of medical genetics. 1995, Vol 32, Num 10, pp 819-822, issn 0022-2593Article