Log on / register
BioMed Central home | Journals A-Z | Feedback | Support | My details
Mechanisms for human genomic rearrangements.
Gu W, Zhang F, Lupski JR
Pathogenetics 2008, 1:4
[Full text] [PubMed] [Related articles] [Cited on BioMed Central]


printer friendly 
to  [Help]

PubMed Central articles that cite the above article:

1.
Disease-causing 7.4 kb cis-regulatory deletion disrupting conserved non-coding sequences and their interaction with the FOXL2 promotor: implications for mutation screening.
D'haene B, Attanasio C, Beysen D, Dostie J, Lemire E, Bouchard P, Field M, Jones K, Lorenz B, Menten B, Buysse K, Pattyn F, Friedli M, Ucla C, Rossier C, Wyss C, Speleman F, De Paepe A, Dekker J, Antonarakis SE, De Baere E
PLoS Genet 2009 Jun, 5:e1000522
 [PubMed Central] [PubMed] [Related articles]
2.
Genomic and genic deletions of the FOX gene cluster on 16q24.1 and inactivating mutations of FOXF1 cause alveolar capillary dysplasia and other malformations.
Stankiewicz P, Sen P, Bhatt SS, Storer M, Xia Z, Bejjani BA, Ou Z, Wiszniewska J, Driscoll DJ, Maisenbacher MK, Bolivar J, Bauer M, Zackai EH, McDonald-McGinn D, Nowaczyk MM, Murray M, Hustead V, Mascotti K, Schultz R, Hallam L, McRae D, Nicholson AG, Newbury R, Durham-O'Donnell J, Knight G, Kini U, Shaikh TH, Martin V, Tyreman M, Simonic I, Willatt L, Paterson J, Mehta S, Rajan D, Fitzgerald T, Gribble S, Prigmore E, Patel A, Shaffer LG, Carter NP, Cheung SW, Langston C, Shaw-Smith C
Am J Hum Genet 2009 Jun, 84:780-91
 [PubMed Central] [PubMed] [Related articles]
3.
Mutations in the heparan-sulfate proteoglycan glypican 6 (GPC6) impair endochondral ossification and cause recessive omodysplasia.
Campos-Xavier AB, Martinet D, Bateman J, Belluoccio D, Rowley L, Tan TY, Baxová A, Gustavson KH, Borochowitz ZU, Innes AM, Unger S, Beckmann JS, Mittaz L, Ballhausen D, Superti-Furga A, Savarirayan R, Bonafé L
Am J Hum Genet 2009 Jun, 84:760-70
 [PubMed Central] [PubMed] [Related articles]
4.
The clinical and biochemical spectrum of congenital adrenal hyperplasia secondary to 21-hydroxylase deficiency.
Huynh T, McGown I, Cowley D, Nyunt O, Leong GM, Harris M, Cotterill AM
Clin Biochem Rev 2009 May, 30:75-86
 [PubMed Central] [PubMed] [Related articles]
5.
Mouse models of genomic syndromes as tools for understanding the basis of complex traits: an example with the smith-magenis and the potocki-lupski syndromes.
Carmona-Mora P, Molina J, Encina CA, Walz K
Curr Genomics 2009 Jun, 10:259-68
 [PubMed Central] [PubMed] [Related articles]
6.
*** Unable to retrieve article 19500772 ***

 [PubMed Central] [PubMed] [Related articles]
7.
Fork stalling and template switching as a mechanism for polyalanine tract expansion affecting the DYC mutant of HOXD13, a new murine model of synpolydactyly.
Cocquempot O, Brault V, Babinet C, Herault Y
Genetics 2009 Sep, 183:23-30
 [PubMed Central] [PubMed] [Related articles]
8.
DNA interstrand crosslink repair in mammalian cells.
McCabe KM, Olson SB, Moses RE
J Cell Physiol 2009 Sep, 220:569-73
 [PubMed Central] [PubMed] [Related articles]
9.
Different molecular mechanisms causing 9p21 deletions in acute lymphoblastic leukemia of childhood.
Novara F, Beri S, Bernardo ME, Bellazzi R, Malovini A, Ciccone R, Cometa AM, Locatelli F, Giorda R, Zuffardi O
Hum Genet 2009 Oct, 126:511-20
 [PubMed Central] [PubMed] [Related articles]
10.
A de novo 8.8-Mb deletion of 21q21.1-q21.3 in an autistic male with a complex rearrangement involving chromosomes 6, 10, and 21.
Haldeman-Englert CR, Chapman KA, Kruger H, Geiger EA, McDonald-McGinn DM, Rappaport E, Zackai EH, Spinner NB, Shaikh TH
Am J Med Genet A 2010 Jan, 152A:196-202
 [PubMed Central] [PubMed] [Related articles]
11.
Mechanisms of copy number variation and hybrid gene formation in the KIR immune gene complex.
Traherne JA, Martin M, Ward R, Ohashi M, Pellett F, Gladman D, Middleton D, Carrington M, Trowsdale J
Hum Mol Genet 2010 Mar 1, 19:737-51
 [PubMed Central] [PubMed] [Related articles]
12.
Roles of retrotransposons in benign and malignant hematologic disease.
Schneider AM, Duffield AS, Symer DE, Burns KH
Cellscience 2009 Oct 27, 6:121-145
 [PubMed Central] [PubMed] [Related articles]

This article is also cited by 1 article in BioMed Central

printer friendly 
to  [Help]
Terms and Conditions Privacy statement Information for advertisers Jobs at BMC Contact us
© 1999-2010 BioMed Central Ltd unless otherwise stated. Part of Springer Science+Business Media.