Detalhe da pesquisa
1.
A high resolution deletion map of human chromosome Xp22.
Nat Genet
; 4(3): 272-9, 1993 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-8358436
2.
Associations with tight junction genes PARD3 and MAGI2 in Dutch patients point to a common barrier defect for coeliac disease and ulcerative colitis.
Gut
; 57(4): 463-7, 2008 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-17989107
3.
Duchenne muscular dystrophy: high frequency of deletions.
Neurology
; 38(1): 1-4, 1988 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-3275902
4.
Molecular-genetic study of Duchenne and Becker muscular dystrophies: deletion analyses of 45 Japanese patients and segregation analyses in their families with RFLPs based on the data from normal Japanese females.
Am J Med Genet
; 34(4): 555-61, 1989 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-2576185
5.
Deletion screening in patients with Duchenne muscular dystrophy.
J Neurol
; 236(8): 470-3, 1989 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-2614492
6.
[Polymorphisms in the pseudoautosomal regions of X and Y in DNA diagnosis]. / Polymorfismy pseudoautosomální oblasti X a Y v DNA diagnostice.
Vnitr Lek
; 39(10): 959-63, 1993 Oct.
Artigo
em Tcheco
| MEDLINE | ID: mdl-8236868
7.
Exon trapping. Application of a large-insert multiple-exon-trapping system.
Methods Mol Biol
; 175: 201-15, 2001.
Artigo
em Inglês
| MEDLINE | ID: mdl-11462836
8.
Isolation and mapping of human chromosome 21 cosmids using a probe for RTVL-H retrovirus-like elements.
Genomics
; 15(3): 492-9, 1993 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-8468043
9.
Molecular deletions in the Duchenne/Becker muscular dystrophy gene.
Clin Genet
; 35(4): 251-60, 1989 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-2653672
10.
Isolation and characterization of cell hybrids containing human Xp-chromosome fragments.
Cytogenet Cell Genet
; 54(1-2): 10-4, 1990.
Artigo
em Inglês
| MEDLINE | ID: mdl-2249469
11.
Isolation of probes detecting restriction fragment length polymorphisms from X chromosome-specific libraries: potential use for diagnosis of Duchenne muscular dystrophy.
Hum Genet
; 70(2): 148-56, 1985.
Artigo
em Inglês
| MEDLINE | ID: mdl-2989153
12.
A YAC-based binning strategy facilitating the rapid assembly of cosmid contigs: 1.6 Mb of overlapping cosmids in Xp22.
Hum Mol Genet
; 3(7): 1155-61, 1994 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-7981686
13.
The genes for X-linked ocular albinism (OA1) and microphthalmia with linear skin defects (MLS): cloning and characterization of the critical regions.
Hum Mol Genet
; 2(7): 947-52, 1993 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-8364577
14.
Characterization of Cxorf5 (71-7A), a novel human cDNA mapping to Xp22 and encoding a protein containing coiled-coil alpha-helical domains.
Genomics
; 51(2): 243-50, 1998 Jul 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-9722947
15.
Direct nonradioactive in situ hybridization of somatic cell hybrid DNA to human lymphocyte chromosomes.
Cytometry
; 11(1): 105-9, 1990.
Artigo
em Inglês
| MEDLINE | ID: mdl-2307050
16.
Physical mapping of 14 new DNA markers isolated from the human distal Xp region.
Genomics
; 13(1): 167-75, 1992 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-1349572
17.
Generation and fluorescent in situ hybridization mapping of yeast artificial chromosomes of 1p, 17p, 17q, and 19q from a hybrid cell line by high-density screening of an amplified library.
Genomics
; 11(4): 1079-87, 1991 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-1783377
18.
The X chromosome shows less genetic variation at restriction sites than the autosomes.
Am J Hum Genet
; 39(4): 438-51, 1986 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-2876629
19.
A gene from the Xp22.3 region shares homology with voltage-gated chloride channels.
Hum Mol Genet
; 3(4): 547-52, 1994 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-8069296
20.
A deletion hot spot in the Duchenne muscular dystrophy gene.
Genomics
; 2(2): 101-8, 1988 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-2900805