Establishment of new human prostatic cancer cell line (JCA-I)
Muraki, Junro, Addonizio, Joseph C., Choudhury, Muhammad S., Fischer, Joel, Eshghi, Majid, Davidian, Marianna M., Shapiro, Lawrence R., Wilmot, Patrick L., Nagamatsu, George R., Chiao, J.W.
Published in Urology (Ridgewood, N.J.) (01.07.1990)
Published in Urology (Ridgewood, N.J.) (01.07.1990)
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Journal Article
Trisomy 5 mosaicism in amniotic fluid with normal outcome
Casamassima, A C, Wilmot, P L, Mahoney, M J, Scott, R V, Shapiro, L R
Published in Clinical genetics (01.04.1989)
Published in Clinical genetics (01.04.1989)
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Journal Article
Kallmann syndrome associated with complex chromosome rearrangement
Casamassima, A C, Wilmot, P L, Vibert, B K, Shapiro, L R
Published in American journal of medical genetics (01.03.1993)
Published in American journal of medical genetics (01.03.1993)
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Journal Article
Pericentric inversion of the Y chromosome and prenatal diagnosis
Shapiro, L R, Pettersen, R O, Wilmot, P L, Warburton, D, Benn, P A, Hsu, L Y
Published in Prenatal diagnosis (01.11.1984)
Published in Prenatal diagnosis (01.11.1984)
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Journal Article
Deletion of 16q with prolonged survival and unusual radiographic manifestations
Casamassima, A C, Klein, R M, Wilmot, P L, Brenholz, P, Shapiro, L R
Published in American journal of medical genetics (01.12.1990)
Published in American journal of medical genetics (01.12.1990)
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Journal Article
Multiple meningiomas in a patient with constitutional ring chromosome 22
Petrella, R, Levine, S, Wilmot, P L, Ashar, K D, Casamassima, A C, Shapiro, L R
Published in American journal of medical genetics (15.08.1993)
Published in American journal of medical genetics (15.08.1993)
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Journal Article
DNA-based genetic testing in fifty fragile X families
Murphy, P D, Watson, M S, Shapiro, L R, Wilmot, P L, Breg, W R
Published in American journal of medical genetics (01.02.1991)
Published in American journal of medical genetics (01.02.1991)
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Journal Article
The karyotype of Philadelphia chromosome-negative, bcr rearrangement-positive chronic myeloid leukemia
Weinstein, M.E., Grossman, A., Perle, M.A., Wilmot, P.L., Verma, R.S., Silver, R.T., Arlin, Z., Allen, S.L., Amorosi, E., Waintraub, S.E., Shapiro, L.R., Benn, P.A.
Published in Cancer genetics and cytogenetics (15.10.1988)
Published in Cancer genetics and cytogenetics (15.10.1988)
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Journal Article
The use of early simultaneous percutaneous umbilical blood sampling (PUBS) and amniocentesis for prenatal fragile X chromosome diagnosis
Butler, M G, Dev, V G, Shah, D, Ulm, J E, Wilmot, P L, Shapiro, L R
Published in American journal of medical genetics (01.12.1988)
Published in American journal of medical genetics (01.12.1988)
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Journal Article
Prenatal diagnosis of fragile X syndrome: results from parallel molecular and cytogenetic studies
Murphy, P D, Wilmot, P L, Shapiro, L R
Published in American journal of medical genetics (15.04.1992)
Published in American journal of medical genetics (15.04.1992)
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Journal Article
Prenatal cytogenetic diagnosis of the fragile X syndrome in amniotic fluid: calculation of accuracy
Shapiro, L R, Wilmot, P L, Fisch, G S
Published in American journal of medical genetics (15.04.1992)
Published in American journal of medical genetics (15.04.1992)
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Journal Article
Experience with multiple approaches to the prenatal diagnosis of the fragile X syndrome: amniotic fluid, chorionic villi, fetal blood and molecular methods
Shapiro, L R, Wilmot, P L, Murphy, P D, Breg, W R
Published in American journal of medical genetics (01.05.1988)
Published in American journal of medical genetics (01.05.1988)
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