Disteche C - Search Results

1

Common trisomy mosaicism diagnosed in amniocytes involving chromosomes 13, 18, 20 and 21: karyotype-phenotype correlations.

Wallerstein R, Yu MT, Neu RL, Benn P, Lee Bowen C, Crandall B, Disteche C, Donahue R, Harrison B, Hershey D, Higgins RR, Jenkins LS, Jackson-Cook C, Keitges E, Khodr G, Lin CC, Luthardt FW, Meisner L, Mengden G, Patil SR, Rodriguez M, Sciorra LJ, Shaffer LG, Stetten G, Van Dyke DL, Wang H. Wallerstein R, et al. Among authors: disteche c. Prenat Diagn. 2000 Feb;20(2):103-22. Prenat Diagn. 2000. PMID: 10694683

2

Is the 15-in situ clone protocol necessary to detect amniotic fluid mosaicism?

Cheng EY, Luthy DA, Dunne DF, Luthardt FW, Disteche CM. Cheng EY, et al. Among authors: disteche cm. Am J Obstet Gynecol. 1995 Oct;173(4):1025-30. doi: 10.1016/0002-9378(95)91321-1. Am J Obstet Gynecol. 1995. PMID: 7485288

3

Rare trisomy mosaicism diagnosed in amniocytes, involving an autosome other than chromosomes 13, 18, 20, and 21: karyotype/phenotype correlations.

Hsu LY, Yu MT, Neu RL, Van Dyke DL, Benn PA, Bradshaw CL, Shaffer LG, Higgins RR, Khodr GS, Morton CC, Wang H, Brothman AR, Chadwick D, Disteche CM, Jenkins LS, Kalousek DK, Pantzar TJ, Wyatt P. Hsu LY, et al. Among authors: disteche cm. Prenat Diagn. 1997 Mar;17(3):201-42. doi: 10.1002/(sici)1097-0223(199703)17:3<201::aid-pd56>3.0.co;2-h. Prenat Diagn. 1997. PMID: 9110367

4

Dosage regulation of the active X chromosome in human triploid cells.

Deng X, Nguyen DK, Hansen RS, Van Dyke DL, Gartler SM, Disteche CM. Deng X, et al. PLoS Genet. 2009 Dec;5(12):e1000751. doi: 10.1371/journal.pgen.1000751. Epub 2009 Dec 4. PLoS Genet. 2009. PMID: 19997486 Free PMC article.

5

Samuel A. Latt, 1938-1988: in memoriam.

Allen J, Disteche C, Heartlein M, Loveday K, Schreck R, Stetten G. Allen J, et al. Among authors: disteche c. Environ Mol Mutagen. 1988;12(4):437-8. Environ Mol Mutagen. 1988. PMID: 3056720 No abstract available.

6

Prenatal identification of a deleted Y chromosome by cytogenetics and a Y-specific repetitive DNA probe.

Disteche C, Luthy D, Haslam DB, Hoar D. Disteche C, et al. Hum Genet. 1984;67(2):222-4. doi: 10.1007/BF00273007. Hum Genet. 1984. PMID: 6745944

7

Fetal t(5p;21q) misdiagnosed as monosomy 21: a plea for in situ hybridization studies.

Gill P, Uhrich S, Disteche C, Cheng E. Gill P, et al. Among authors: disteche c. Am J Med Genet. 1994 Oct 1;52(4):416-8. doi: 10.1002/ajmg.1320520405. Am J Med Genet. 1994. PMID: 7747753

8

Analysis of a paracentric inversion in human oocytes: nonhomologous pairing in pachytene.

Cheng EY, Chen YJ, Disteche CM, Gartler SM. Cheng EY, et al. Among authors: disteche cm. Hum Genet. 1999 Sep;105(3):191-6. doi: 10.1007/s004399900120. Hum Genet. 1999. PMID: 10987644

9

Karyotype/phenotype correlations in duplication 4q: evidence for a critical region within 4q27-28 for preaxial defects.

Battaglia A, Chen Z, Brothman AR, Morelli S, Palumbos JC, Carey JC, Hudgins L, Disteche C. Battaglia A, et al. Among authors: disteche c. Am J Med Genet A. 2005 Apr 30;134(3):334-7. doi: 10.1002/ajmg.a.30644. Am J Med Genet A. 2005. PMID: 15759263 No abstract available.

10

TCR selection and allelic exclusion in RAG transgenic mice that exhibit abnormal T cell localization in lymph nodes and lymphatics.

Wayne J, Suh H, Sokol KA, Petrie HT, Witmer-Pack M, Edelhoff S, Disteche CM, Nussenzweig MC. Wayne J, et al. Among authors: disteche cm. J Immunol. 1994 Dec 15;153(12):5491-502. J Immunol. 1994. PMID: 7989751

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