Report of the third international workshop on human chromosome 15 mapping 1996

Cytogenetics and Cell Genetics

Volumn 76, Issue 1-2, 1997, Pages 2-13

  Robinson, W P ^a   Horsthemke, B ^b   Leonard, S ^b   Malcolm, S ^b   Morton, C ^b   Nicholls, R D ^b   Ritchie, R J ^b   Rogan, P ^b   Schultz, R ^b   Schwartz, S ^b   Sharp, J ^b   Trent, R ^b   Wevrick, R ^b   Williamson, M ^b   Knoll, J H M ^b  

^a UNIVERSITY OF BRITISH COLUMBIA   (Canada)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

CHROMOSOME 15; CHROMOSOME BREAKAGE; CHROMOSOME MAP; CONFERENCE PAPER; DELETION MUTANT; GENE DUPLICATION; GENE MAPPING; HUMAN; PRIORITY JOURNAL; WORKSHOP;

EID: 0030895426     PISSN: 03010171     EISSN: None     Source Type: Journal    
DOI: 10.1159/000134500     Document Type: Conference Paper

References (32)

1. Allamand V, Broux O, Richard I, Fougerousse F, Chiannilkulchai N, Bourg N, Brenguier L, Devaud C, Pasturaud P, Pereira de Souza A, et al: Preferential localization of the limb-girdle muscular dystrophy type 2A gene in the proximal part of a 1-cM 15q15.1→q15.3 interval. Am J hum Genet 56:1417-30 (1995).
2. Beckmann JS, Tomfohrde J, Barnes RI, Williams M, Broux O, Richard I, Weissenbach J, Bowcock AM: A linkage map of human chromosome 15 with an average resolution of 2 cM and containing 55 polymorphic microsatellites. Hum Mol Genet 2:2019-30 (1993).
3. Buiting K, Greger V, Brownstein BH, Mohr RM, Voiculescu I, Winterpacht A, Zabel B, et al: A putative gene family in 15q11→q13 and 16p11.2: possible implications for Prader-Willi and Angelman syndromes. Proc natl Acad Sci, USA 89:5457-61 (1992).
4. Buiting K, Dittrich, B, Endele S, Horsthemke B: Identification of novel exons 3′ to the human SNRPN gene. Genomics, in press (1997).
5. Butler MG, Rogan PK: Atypical clinical findings in Prader-Willi syndrome patients: Analysis of survey data. Prader-Willi Perspectives 4:3-6 (1996).
6. Chiannilkulchai N, Pasturaud P, Richard I, Auffray C, Beckmann JS: A primary expression map of the chromosome 15q15 region containing the recessive form of limb-girdle muscular dystrophy (LGMD2A) gene. Hum Mol Genet 4:717-25 (1995).
7. Christian SL, Robinson WP, Mutirangura A, Line MR, Nakao M, Chakravarti A, Surti U, Ledbetter DH: Molecular characterization of two proximal deletion breakpoints in both Prader-Willi and Angelman Syndrome patients. Am J hum Genet 57:40-48 (1995).
8. Dittrich B, Buiting K, Korn B, Richards S, Buxton J, Saitoh S, Nicholls RD, Poustka A, Winterpacht A, Zabel B, Horsthemke B: Imprint switching on human chromosome 15 may involve alternative transcripts of the SNRPN gene. Nature Genet 14:163-170 (1996).
9. Donahue LR, Faust JR, Bronson RT: A new mouse model of Batten Disease, neuronal ceroid lipofuscinosis (Nclf), maps to chromosome nine. Abstract from the 10th International Mouse Genome Conference Oct 7-10, 1996, Institut Pasteur, France (1996).
10. Donlon TA, Morton CC: Report of the committee on the genetic constitution of chromosome 15, in Cuticchia AJ (ed): Human Genome Mapping 1995: A Compendium, pp 862-886 (Johns Hopkins University Press, Baltimore 1996).
11. Eiberg H, Mohr J: Assignment of genes coding for brown eye colour (BEY2) and brown hair color (HCL3) on chromosome 15q. Eur J Hum Genet 4:237-241 (1996).
12. Fougerousse F, Broux O, Richard I, Allamand V, de Souza AP, Bourg N, Brenguier L, Devaud C, Pasturaud P, Roudaut C, et al: Mapping of a chromosome 15 region involved in limb girdle muscular dystrophy. Hum Mol Genet 3:285-93 (1994).
13. Gunaratne PH, Nakao M, Ledbetter DH, Sutcliffe J, Chinault AC: Tissue specific and allele-specific replication timing control in the imprinted human Prader-Willi Syndrome region. Genes Dev 9:808-820 (1995).
14. Holm VA, Cassidy SB, Butler MG, Hanchett JM, Greenswag LR, Whitman BY, Greenberg F: Prader-Willi syndrome: Consensus diagnostic criteria. Pediatrics 91:398-402 (1993).
15. Jaiswal AK, Nebert DW, McBride OW, Gonzalez FJ: Human P(3)450: cDNA and complete protein sequence, repetitive Alu sequences in the 3′ nontranslated region, and localization of gene to chromosome 15. J Exp Pathol 3:1-17 (1987).
16. Kishino T, Lalande M, Wagstaff J: UBE3A/E6-AP mutations cause Angelman Syndrome. Nature Genet 15: in press (1997).
17. Knoll JHM, Nicholls RD, Magenis RD, Glatt K, Graham JM, Kaplan L, Lalande M: Angelman syndrome: three molecular classes identifed with chromosome 15q11→q13-specific DNA markers. Am J hum Genet 47:149-155 (1990).
18. Lee S-T, Nicholls RD, Bundey S, Laxova R, Musarella M, Spritz RA: Mutations of the P gene in oculocutaneous albinism, ocular albinism and Prader-Willi syndrome plus albinism. New Engl J Med 330:529-534 (1994).
19. Malcolm S, Donlon TA: Report and abstracts of the Second International Workshop on Human Chromosome 15 Mapping. Cytogenet Cell Genet 67:1-22 (1994).
20. McDaniel LD, Zhang B, Kubiczek E, Ritter M, Huang J, Berard C, Leana-Cox J, Schwartz S, Schultz RA. Construction and screening of a cosmid library generated from a somatic cell hybrid bearing human chromosome 15. Genomics: in press (1997).
21. Mohandas TK, Chen X-N, Rowe LB, Birkenmeier EH, Fanning AS, Anderson JM, Korenberg JR: Localization of the tight junction protein gene TJP1 to human chromosome 15q13, distal to the Prader-Willi/Angelman region, and to mouse chromosome 7. Genomics 30:594-597 (1995).
22. Nakao M, Sutcliffe JS, Durtschi B, Mutirangura A, Ledbetter DH, Beaudet AL: Imprinting analysis of three genes in the Prader-Willi/Angelman region: SNRPN, E6-associated protein, and PAR-2 (D15S225E). Hum Molec Genet 3:309-315 (1994).
23. Ning Y, Roschke A, Christian SL, Lesser J, Sutcliffe JS, Ledbetter DH: Identification of a novel paternally expressed transcript adjacent to snRPN in the Prader-Willi syndrome critical region. Genome Res 6:742-746 (1996).
24. Richard I, Roudaut C, Fougerousse F, Chiannilkulchai N, Beckmann JS: An STS map of the limb girdle muscular dystrophy type 2A region. Mammal Genome 6:754-6 (1995).
25. Rogan PK, Butler MG: Atypical clinical findings in PWS patients: A survey. Prader-Willi Perspectives 2:13-16 (1994).
26. Rogan PK, Seip JR, Driscoll DJ, Papenhausen PR, Johnson VP, Raaskin S, Woodward AM, Butler MG: Distinct 15q genotypes in Russell-Silver and Ring 15 syndromes. Am J Med Genet 62:10-15 (1996).
27. Saitoh, S.B., Buiting K, Rogan, PK, et al.: Minimal definition of the imprinting center and fixation of a chromosome 15q11→q13 epigenotype by imprinting mutations. Proc natl Acad Sci, (USA) 93:7811-7815 (1996).
28. Straughen J, Ciocci S, Ye T-Z, Lennon DN, Proytcheva M, Alhadeff B, Goodfellow P, German J, Ellis NA, Groden J: Physical mapping of the Bloom syndrome region by the identification of YAC and P1 clones from human chromosome 15 band q26.1. Genomics 35:118-128 (1996).
29. Wevrick R, Kerns J, Francke U: Identification of a novel paternally expressed gene in the Prader-Willi syndrome region. Hum Mol Genet 3:1877-1882 (1994).
30. Wevrick R, Francke U: An imprinted mouse transcript homologous to the human Imprinted in Prader-Willi syndrome (IPW) gene. Hum molec Gen, in press (1997).
31. White LM, Rogan PK, Nicholls RD, Wu B-L, Korf B, Knoll JHM: Allele-specific replication timing of 15q11→q13 loci: a diagnostic test for detection of uniparental disomy. Am J hum Genet 59:423-430 (1996).
32. Woodage T, Prasad M, Dixon JW, Selby RE, Roman DR, Columbano-Green LM, Graham D, Rogan PK, Seip JR, Smith A, Trent RJ: Bloom syndrome and maternal uniparental disomy for chromosome 15. Am J hum Genet 55:74-80 (1994).