Precht KS[au] - Search Results

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Year	Number of Results
1998	2
1999	1
2000	1
2022	0

Page 1

Satellited chromosome 10 detected prenatally in a fetus and confirmed as mosaic in a parent.

Storto PD, Diehn TN, O'Malley DP, Bullard BA, Netzloff ML, VanDyke DL, Feldman GL, Precht KS, Ledbetter DH, Lese CM. Storto PD, et al. Among authors: precht ks. Prenat Diagn. 1999 Nov;19(11):1088-9. doi: 10.1002/(sici)1097-0223(199911)19:11<1088::aid-pd692>3.0.co;2-r. Prenat Diagn. 1999. PMID: 10589072 No abstract available.

Two 22q telomere deletions serendipitously detected by FISH.

Precht KS, Lese CM, Spiro RP, Huttenlocher PR, Johnston KM, Baker JC, Christian SL, Kittikamron K, Ledbetter DH. Precht KS, et al. J Med Genet. 1998 Nov;35(11):939-42. doi: 10.1136/jmg.35.11.939. J Med Genet. 1998. PMID: 9832042 Free PMC article.

An optimized set of human telomere clones for studying telomere integrity and architecture.

Knight SJ, Lese CM, Precht KS, Kuc J, Ning Y, Lucas S, Regan R, Brenan M, Nicod A, Lawrie NM, Cardy DL, Nguyen H, Hudson TJ, Riethman HC, Ledbetter DH, Flint J. Knight SJ, et al. Among authors: precht ks. Am J Hum Genet. 2000 Aug;67(2):320-32. doi: 10.1086/302998. Epub 2000 Jun 22. Am J Hum Genet. 2000. PMID: 10869233 Free PMC article.

Fluorescence in situ hybridization analysis with LIS1 specific probes reveals a high deletion mutation rate in isolated lissencephaly sequence.

Pilz DT, Macha ME, Precht KS, Smith AC, Dobyns WB, Ledbetter DH. Pilz DT, et al. Among authors: precht ks. Genet Med. 1998 Nov-Dec;1(1):29-33. doi: 10.1097/00125817-199811000-00007. Genet Med. 1998. PMID: 11261426 Free article.

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