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Items: 1 to 20 of 143

1.

Characterisation of the exon structure of the Fanconi anaemia group C gene by vectorette PCR.

Gibson RA, Buchwald M, Roberts RG, Mathew CG.

Hum Mol Genet. 1993 Jan;2(1):35-8.

PMID:
8490620
2.

Characterization of the 5' region of the Fanconi anaemia group C (FACC) gene.

Savoia A, Centra M, Ianzano L, de Cillis GP, Zelante L, Buchwald M.

Hum Mol Genet. 1995 Aug;4(8):1321-6.

PMID:
7581369
3.

A common mutation in the FACC gene causes Fanconi anaemia in Ashkenazi Jews.

Whitney MA, Saito H, Jakobs PM, Gibson RA, Moses RE, Grompe M.

Nat Genet. 1993 Jun;4(2):202-5.

PMID:
8348157
4.

A nonsense mutation and exon skipping in the Fanconi anaemia group C gene.

Gibson RA, Hajianpour A, Murer-Orlando M, Buchwald M, Mathew CG.

Hum Mol Genet. 1993 Jun;2(6):797-9.

PMID:
7689011
5.

Determination of the exon structure of the distal portion of the dystrophin gene by vectorette PCR.

Roberts RG, Coffey AJ, Bobrow M, Bentley DR.

Genomics. 1992 Aug;13(4):942-50.

PMID:
1505985
6.
7.

Mutation analysis of the Fanconi anemia gene FACC.

Verlander PC, Lin JD, Udono MU, Zhang Q, Gibson RA, Mathew CG, Auerbach AD.

Am J Hum Genet. 1994 Apr;54(4):595-601.

8.

Molecular characterization of three novel Fanconi anemia mutations in Israeli Arabs.

Tamary H, Dgany O, Toledano H, Shalev Z, Krasnov T, Shalmon L, Schechter T, Bercovich D, Attias D, Laor R, Koren A, Yaniv I.

Eur J Haematol. 2004 May;72(5):330-5.

PMID:
15059067
9.
10.

The genomic structure of two protein kinase CK2alpha genes of Xenopus laevis and features of the putative promoter region.

Wilhelm V, Neckelman G, Allende JE, Allende CC.

Mol Cell Biochem. 2001 Nov;227(1-2):175-83.

PMID:
11827169
11.

Cloning of cDNAs for Fanconi's anaemia by functional complementation.

Strathdee CA, Gavish H, Shannon WR, Buchwald M.

Nature. 1992 Apr 30;356(6372):763-7. Erratum in: Nature. 1992 Jul 30;358(6385):434.

PMID:
1574115
12.

Exon amplification: a strategy to isolate mammalian genes based on RNA splicing.

Buckler AJ, Chang DD, Graw SL, Brook JD, Haber DA, Sharp PA, Housman DE.

Proc Natl Acad Sci U S A. 1991 May 1;88(9):4005-9.

13.
14.

Exon structure of the human dystrophin gene.

Roberts RG, Coffey AJ, Bobrow M, Bentley DR.

Genomics. 1993 May;16(2):536-8.

PMID:
8314593
15.

Genomic organization of the neurofibromatosis 1 gene (NF1).

Li Y, O'Connell P, Breidenbach HH, Cawthon R, Stevens J, Xu G, Neil S, Robertson M, White R, Viskochil D.

Genomics. 1995 Jan 1;25(1):9-18.

PMID:
7774960
16.

The genomic organization of the Fanconi anemia group A (FAA) gene.

Ianzano L, D'Apolito M, Centra M, Savino M, Levran O, Auerbach AD, Cleton-Jansen AM, Doggett NA, Pronk JC, Tipping AJ, Gibson RA, Mathew CG, Whitmore SA, Apostolou S, Callen DF, Zelante L, Savoia A.

Genomics. 1997 May 1;41(3):309-14.

PMID:
9169126
17.

Identification of intron/exon boundaries in genomic DNA by inverse PCR.

Albertsen H, Thliveris A.

Curr Protoc Hum Genet. 2001 May;Chapter 6:Unit 6.4. doi: 10.1002/0471142905.hg0604s00.

PMID:
18428300
18.

Complete exon-intron organization and chromosomal location of the gene for mouse type XIII collagen (col13a1) and comparison with its human homologue.

Kvist AP, Latvanlehto A, Sund M, Horelli-Kuitunen N, Rehn M, Palotie A, Beier D, Pihlajaniemi T.

Matrix Biol. 1999 Jun;18(3):261-74.

PMID:
10429945
19.

Fanconi anemia in Tunisia: high prevalence of group A and identification of new FANCA mutations.

Bouchlaka C, Abdelhak S, Amouri A, Ben Abid H, Hadiji S, Frikha M, Ben Othman T, Amri F, Ayadi H, Hachicha M, Rebaï A, Saad A, Dellagi K; Tunisian Fanconi Anemia Study Group.

J Hum Genet. 2003;48(7):352-61. Epub 2003 Jun 24.

PMID:
12827451
20.

Molecular cloning of the mouse gene coding for carbonic anhydrase IV.

Tamai S, Cody LB, Sly WS.

Biochem Genet. 1996 Feb;34(1-2):31-43.

PMID:
8935991
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