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Trisomy 16 and trisomy 16 Mosaicism: a review.
Benn P. Benn P. Am J Med Genet. 1998 Sep 1;79(2):121-33. Am J Med Genet. 1998. PMID: 9741470 Review.
Proposed guidelines for diagnosis of chromosome mosaicism in amniocytes based on data derived from chromosome mosaicism and pseudomosaicism studies.
Hsu LY, Kaffe S, Jenkins EC, Alonso L, Benn PA, David K, Hirschhorn K, Lieber E, Shanske A, Shapiro LR, et al. Hsu LY, et al. Among authors: benn pa. Prenat Diagn. 1992 Jul;12(7):555-73. doi: 10.1002/pd.1970120702. Prenat Diagn. 1992. PMID: 1508847
The centralized prenatal genetics screening program of New York City III: The first 7,000 cases.
Benn PA, Hsu LY, Carlson A, Tannenbaum HL. Benn PA, et al. Am J Med Genet. 1985 Feb;20(2):369-84. doi: 10.1002/ajmg.1320200221. Am J Med Genet. 1985. PMID: 2579556
The administrative aspects of the establishment of the laboratory were described in papers I [Hsu, 1981] and II [Hsu and Benn, 1981] in this series. ...
The administrative aspects of the establishment of the laboratory were described in papers I [Hsu, 1981] and II [Hsu and Benn, 1981] …
Incidence and significance of supernumerary marker chromosomes in prenatal diagnosis.
Benn PA, Hsu LY. Benn PA, et al. Am J Hum Genet. 1984 Sep;36(5):1092-102. Am J Hum Genet. 1984. PMID: 6594043 Free PMC article.
Prenatal diagnosis of chromosome mosaicism.
Benn P, Hsu LY, Perlis T, Schonhaut A. Benn P, et al. Prenat Diagn. 1984 Jan-Feb;4(1):1-9. doi: 10.1002/pd.1970040102. Prenat Diagn. 1984. PMID: 6728823
A high incidence of maternal cell contamination of amniotic fluid cell cultures.
Benn PA, Schonhaut AG, Hsu LY. Benn PA, et al. Am J Med Genet. 1983 Feb;14(2):361-5. doi: 10.1002/ajmg.1320140216. Am J Med Genet. 1983. PMID: 6837631 No abstract available.
Prenatal diagnosis of diverse chromosome abnormalities in a population of patients identified by triple-marker testing as screen positive for Down syndrome.
Benn PA, Horne D, Briganti S, Greenstein RM. Benn PA, et al. Am J Obstet Gynecol. 1995 Aug;173(2):496-501. doi: 10.1016/0002-9378(95)90272-4. Am J Obstet Gynecol. 1995. PMID: 7544068
Comparison of high resolution chromosome banding and fluorescence in situ hybridization (FISH) for the laboratory evaluation of Prader-Willi syndrome and Angelman syndrome.
Delach JA, Rosengren SS, Kaplan L, Greenstein RM, Cassidy SB, Benn PA. Delach JA, et al. Among authors: benn pa. Am J Med Genet. 1994 Aug 1;52(1):85-91. doi: 10.1002/ajmg.1320520117. Am J Med Genet. 1994. PMID: 7977469
Variable clinical expression of mosaic trisomy 16 in the newborn infant.
Devi AS, Velinov M, Kamath MV, Eisenfeld L, Neu R, Ciarleglio L, Greenstein R, Benn P. Devi AS, et al. Among authors: benn p. Am J Med Genet. 1993 Aug 15;47(2):294-8. doi: 10.1002/ajmg.1320470231. Am J Med Genet. 1993. PMID: 8213923 Review.
Review of the cytogenetic changes in acute megakaryoblastic leukemia: one disease or several?
Lu G, Altman AJ, Benn PA. Lu G, et al. Among authors: benn pa. Cancer Genet Cytogenet. 1993 Jun;67(2):81-9. doi: 10.1016/0165-4608(93)90157-h. Cancer Genet Cytogenet. 1993. PMID: 8330276
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