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Methylation-specific PCR simplifies imprinting analysis.
Kubota T, Das S, Christian SL, Baylin SB, Herman JG, Ledbetter DH. Kubota T, et al. Among authors: christian sl. Nat Genet. 1997 May;16(1):16-7. doi: 10.1038/ng0597-15. Nat Genet. 1997. PMID: 9140389 No abstract available.
Validation studies of SNRPN methylation as a diagnostic test for Prader-Willi syndrome.
Kubota T, Sutcliffe JS, Aradhya S, Gillessen-Kaesbach G, Christian SL, Horsthemke B, Beaudet AL, Ledbetter DH. Kubota T, et al. Among authors: christian sl. Am J Med Genet. 1996 Dec 2;66(1):77-80. doi: 10.1002/(SICI)1096-8628(19961202)66:1<77::AID-AJMG18>3.0.CO;2-N. Am J Med Genet. 1996. PMID: 8957518
Report of the fourth international workshop on human chromosome 15 mapping 1997.
Morton CC, Christian SL, Donlon TA, Driscoll DJ, Fink JK, Gabriel JM, Gotway G, Greally JM, Hitchins MP, Howard HC, Ji Y, Leonard S, Lerner T, Magenis E, Malcolm S, Ohta T, Rainier S, Rees M, Riley B, Robinson WP, Saitoh S, Schultz R, Sell S, Sharp JD, Nicholls RD, et al. Morton CC, et al. Among authors: christian sl. Cytogenet Cell Genet. 1999;84(1-2):12-21. doi: 10.1159/000015203. Cytogenet Cell Genet. 1999. PMID: 10343092 No abstract available.
Molecular screening for proximal 15q abnormalities in a mentally retarded population.
Jacobsen J, King BH, Leventhal BL, Christian SL, Ledbetter DH, Cook EH Jr. Jacobsen J, et al. Among authors: christian sl. J Med Genet. 1998 Jul;35(7):534-8. doi: 10.1136/jmg.35.7.534. J Med Genet. 1998. PMID: 9678696 Free PMC article.
Inter- and intrachromosomal rearrangements are both involved in the origin of 15q11-q13 deletions in Prader-Willi syndrome.
Carrozzo R, Rossi E, Christian SL, Kittikamron K, Livieri C, Corrias A, Pucci L, Fois A, Simi P, Bosio L, Beccaria L, Zuffardi O, Ledbetter DH. Carrozzo R, et al. Among authors: christian sl. Am J Hum Genet. 1997 Jul;61(1):228-31. doi: 10.1086/513907. Am J Hum Genet. 1997. PMID: 9246004 Free PMC article. 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. Among authors: christian sl. 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.
Integrated YAC contig map of the Prader-Willi/Angelman region on chromosome 15q11-q13 with average STS spacing of 35 kb.
Christian SL, Bhatt NK, Martin SA, Sutcliffe JS, Kubota T, Huang B, Mutirangura A, Chinault AC, Beaudet AL, Ledbetter DH. Christian SL, et al. Genome Res. 1998 Feb;8(2):146-57. doi: 10.1101/gr.8.2.146. Genome Res. 1998. PMID: 9477342 Free PMC article.
Robertsonian (15q;15q) translocation in a child with Angelman syndrome: evidence of uniparental disomy.
Tonk V, Schultz RA, Christian SL, Kubota T, Ledbetter DH, Wilson GN. Tonk V, et al. Among authors: christian sl. Am J Med Genet. 1996 Dec 30;66(4):426-8. doi: 10.1002/(SICI)1096-8628(19961230)66:4<426::AID-AJMG7>3.0.CO;2-I. Am J Med Genet. 1996. PMID: 8989460
Prenatal diagnosis of uniparental disomy 15 following trisomy 15 mosaicism.
Christian SL, Smith AC, Macha M, Black SH, Elder FF, Johnson JM, Resta RG, Surti U, Suslak L, Verp MS, Ledbetter DH. Christian SL, et al. Prenat Diagn. 1996 Apr;16(4):323-32. doi: 10.1002/(SICI)1097-0223(199604)16:4<323::AID-PD856>3.0.CO;2-5. Prenat Diagn. 1996. PMID: 8734806
Large genomic duplicons map to sites of instability in the Prader-Willi/Angelman syndrome chromosome region (15q11-q13).
Christian SL, Fantes JA, Mewborn SK, Huang B, Ledbetter DH. Christian SL, et al. Hum Mol Genet. 1999 Jun;8(6):1025-37. doi: 10.1093/hmg/8.6.1025. Hum Mol Genet. 1999. PMID: 10332034
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