Simpson JL - Search Results

1

Mutations in the conserved domain of SRY are uncommon in XY gonadal dysgenesis.

Pivnick EK, Wachtel S, Woods D, Simpson JL, Bishop CE. Pivnick EK, et al. Among authors: simpson jl. Hum Genet. 1992 Nov;90(3):308-10. doi: 10.1007/BF00220087. Hum Genet. 1992. PMID: 1487248

2

Fetal cells in the maternal circulation: isolation by multiparameter flow cytometry and confirmation by polymerase chain reaction.

Wachtel S, Elias S, Price J, Wachtel G, Phillips O, Shulman L, Meyers C, Simpson JL, Dockter M. Wachtel S, et al. Among authors: simpson jl. Hum Reprod. 1991 Nov;6(10):1466-9. doi: 10.1093/oxfordjournals.humrep.a137290. Hum Reprod. 1991. PMID: 1770146

3

Inability to detect fetal metaphases in flow-sorted lymphocyte cultures based on maternal-fetal HLA differences.

Tharapel AT, Jaswaney VL, Dockter ME, Wachtel SS, Chandler RW, Simpson JL, Shulman LP, Meyers CM, Elias S. Tharapel AT, et al. Among authors: simpson jl. Fetal Diagn Ther. 1993 Mar-Apr;8(2):95-101. doi: 10.1159/000263755. Fetal Diagn Ther. 1993. PMID: 8338631

4

Lack of heritability in ovarian germ cell malignancies.

Shulman LP, Muram D, Marina N, Jones C, Portera JC, Wachtel SS, Simpson JL, Elias S. Shulman LP, et al. Among authors: simpson jl. Am J Obstet Gynecol. 1994 Jun;170(6):1803-5; discussion 1805-8. doi: 10.1016/s0002-9378(94)70356-6. Am J Obstet Gynecol. 1994. PMID: 8203441

5

XY gonadal dysgenesis: genetic heterogeneity based upon clinical observations, H-Y antigen status and segregation analysis.

Simpson JL, Blagowidow N, Martin AO. Simpson JL, et al. Hum Genet. 1981;58(1):91-7. doi: 10.1007/BF00284155. Hum Genet. 1981. PMID: 7286997

6

Growth differentiating factor-9 mutations may be associated with premature ovarian failure.

Kovanci E, Rohozinski J, Simpson JL, Heard MJ, Bishop CE, Carson SA. Kovanci E, et al. Among authors: simpson jl. Fertil Steril. 2007 Jan;87(1):143-6. doi: 10.1016/j.fertnstert.2006.05.079. Epub 2006 Dec 6. Fertil Steril. 2007. PMID: 17156781 Free article.

7

Sister chromatid exchange (SCE) frequencies differ between directly prepared cytotrophoblasts and cultured mesenchymal core cells.

Shulman LP, Li LR, Tharapel AT, Simpson JL, Elias S. Shulman LP, et al. Among authors: simpson jl. Hum Genet. 1991 Oct;87(6):734-6. doi: 10.1007/BF00201736. Hum Genet. 1991. PMID: 1937478

8

Failure to document fetal cells in maternal circulation using the Selypes-Lorencz "air-culture" cytogenetic technique.

Youssef M, Shulman LP, Tharapel AT, Simpson JL, Elias S. Youssef M, et al. Among authors: simpson jl. Hum Genet. 1990 Jun;85(1):133-4. doi: 10.1007/BF00276341. Hum Genet. 1990. PMID: 2358297

9

Deletion (X)(q26.1-->q28) in a proband and her mother: molecular characterization and phenotypic-karyotypic deductions.

Tharapel AT, Anderson KP, Simpson JL, Martens PR, Wilroy RS Jr, Llerena JC Jr, Schwartz CE. Tharapel AT, et al. Among authors: simpson jl. Am J Hum Genet. 1993 Mar;52(3):463-71. Am J Hum Genet. 1993. PMID: 8095365 Free PMC article.

10

First trimester prenatal diagnosis of trisomy 21 in fetal cells from maternal blood.

Elias S, Price J, Dockter M, Wachtel S, Tharapel A, Simpson JL, Klinger KW. Elias S, et al. Among authors: simpson jl. Lancet. 1992 Oct 24;340(8826):1033. doi: 10.1016/0140-6736(92)93041-k. Lancet. 1992. PMID: 1357416 No abstract available.

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