Schlessinger D - Search Results

1

Refinement of the background genetic map of Xq26-q27 and gene localisation for Börjeson-Forssman-Lehmann Syndrome.

Gedeon AK, Kozman HM, Robinson H, Pilia G, Schlessinger D, Turner G, Mulley JC. Gedeon AK, et al. Among authors: schlessinger d. Am J Med Genet. 1996 Jul 12;64(1):63-8. doi: 10.1002/(SICI)1096-8628(19960712)64:1<63::AID-AJMG9>3.0.CO;2-S. Am J Med Genet. 1996. PMID: 8826450

2

Yeast artificial chromosomes spanning 8 megabases and 10-15 centimorgans of human cytogenetic band Xq26.

Little RD, Pilia G, Johnson S, D'Urso M, Schlessinger D. Little RD, et al. Among authors: d urso m, schlessinger d. Proc Natl Acad Sci U S A. 1992 Jan 1;89(1):177-81. doi: 10.1073/pnas.89.1.177. Proc Natl Acad Sci U S A. 1992. PMID: 1729687 Free PMC article.

3

BLOCK-based PCR markers to find gene family members in human and comparative genome analysis.

D'Esposito M, Pilia G, Schlessinger D. D'Esposito M, et al. Among authors: schlessinger d. Hum Mol Genet. 1994 May;3(5):735-40. doi: 10.1093/hmg/3.5.735. Hum Mol Genet. 1994. PMID: 7915930

4

YAC/STS map of 9 Mb of Xq26 at 100-kb resolution, localizing 6 ESTs, 6 genes, and 32 genetic markers.

Pilia G, MacMillan S, Nagaraja R, Mumm S, Weissenbach J, Schlessinger D. Pilia G, et al. Among authors: schlessinger d. Genomics. 1996 May 15;34(1):55-62. doi: 10.1006/geno.1996.0240. Genomics. 1996. PMID: 8661023

5

Large scale deletions in the GPC3 gene may account for a minority of cases of Simpson-Golabi-Behmel syndrome.

Lindsay S, Ireland M, O'Brien O, Clayton-Smith J, Hurst JA, Mann J, Cole T, Sampson J, Slaney S, Schlessinger D, Burn J, Pilia G. Lindsay S, et al. Among authors: schlessinger d. J Med Genet. 1997 Jun;34(6):480-3. doi: 10.1136/jmg.34.6.480. J Med Genet. 1997. PMID: 9192268 Free PMC article.

6

Fragile X genotype characterized by an unstable region of DNA.

Yu S, Pritchard M, Kremer E, Lynch M, Nancarrow J, Baker E, Holman K, Mulley JC, Warren ST, Schlessinger D, et al. Yu S, et al. Among authors: schlessinger d. Science. 1991 May 24;252(5009):1179-81. doi: 10.1126/science.252.5009.1179. Science. 1991. PMID: 2031189

7

A submicroscopic deletion in Xq26 associated with familial situs ambiguus.

Ferrero GB, Gebbia M, Pilia G, Witte D, Peier A, Hopkin RJ, Craigen WJ, Shaffer LG, Schlessinger D, Ballabio A, Casey B. Ferrero GB, et al. Among authors: schlessinger d. Am J Hum Genet. 1997 Aug;61(2):395-401. doi: 10.1086/514857. Am J Hum Genet. 1997. PMID: 9311745 Free PMC article.

8

Construction of a YAC contig and an STS map spanning 3.6 megabase pairs in Xp22.1.

Trump D, Pilia G, Dixon PH, Wooding C, Thakrar R, Leigh SE, Nagaraja R, Whyte MP, Schlessinger D, Thakker RV. Trump D, et al. Among authors: schlessinger d. Hum Genet. 1996 Jan;97(1):60-8. doi: 10.1007/BF00218834. Hum Genet. 1996. PMID: 8557262

9

Mutations in GPC3, a glypican gene, cause the Simpson-Golabi-Behmel overgrowth syndrome.

Pilia G, Hughes-Benzie RM, MacKenzie A, Baybayan P, Chen EY, Huber R, Neri G, Cao A, Forabosco A, Schlessinger D. Pilia G, et al. Among authors: schlessinger d. Nat Genet. 1996 Mar;12(3):241-7. doi: 10.1038/ng0396-241. Nat Genet. 1996. PMID: 8589713

10

YAC/STS map across 12 Mb of Xq27 at 25-kb resolution, merging Xq26-qter.

Zucchi I, Mumm S, Pilia G, Macmillan S, Reinbold R, Susani L, Weissenbach J, Schlessinger D. Zucchi I, et al. Among authors: schlessinger d. Genomics. 1996 May 15;34(1):42-54. doi: 10.1006/geno.1996.0239. Genomics. 1996. PMID: 8661022

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