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Trisomy 16 mosaicism in amniotic fluid cell cultures.
Tantravahi U, Matsumoto C, Delach J, Craffey A, Smeltzer J, Benn P. Tantravahi U, et al. Among authors: benn p. Prenat Diagn. 1996 Aug;16(8):749-54. doi: 10.1002/(SICI)1097-0223(199608)16:8<749::AID-PD935>3.0.CO;2-C. Prenat Diagn. 1996. PMID: 8878286
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
Fetal blood sampling in investigation of chromosome mosaicism in amniotic fluid cell culture.
Kaffe S, Benn PA, Hsu LY. Kaffe S, et al. Among authors: benn pa. Lancet. 1988 Jul 30;2(8605):284. doi: 10.1016/s0140-6736(88)92581-0. Lancet. 1988. PMID: 2899277 No abstract available.
Evidence for preferential involvement of chromosome bands 6p21 and 13q14 in amniotic fluid cell balanced translocation pseudomosaicism.
Benn PA, Hsu LY. Benn PA, et al. Clin Genet. 1986 Feb;29(2):116-21. doi: 10.1111/j.1399-0004.1986.tb01233.x. Clin Genet. 1986. PMID: 3955861
Maternal cell contamination of amniotic fluid cell cultures: results of a U.S. nationwide survey.
Benn PA, Hsu LY. Benn PA, et al. Am J Med Genet. 1983 Jun;15(2):297-305. doi: 10.1002/ajmg.1320150213. Am J Med Genet. 1983. PMID: 6349361 No abstract available.
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
Maternal cell contamination of amniotic fluid cell cultures from two consecutive pregnancies complicated by fibroids.
Benn PA, Gilbert F, Hsu LY. Benn PA, et al. Prenat Diagn. 1984 Mar-Apr;4(2):151-3. doi: 10.1002/pd.1970040211. Prenat Diagn. 1984. PMID: 6739438
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
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.
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