YAC CONTIGS IN XQ12-]Q13.1

YAC CONTIGS IN XQ12-]Q13.1

Sonraí bibleagrafaíochta
Príomhchruthaitheoirí:	Rider, S, Fairweather, N, Chelly, J, Wagner, T, Muller, U, Monaco, A
Formáid:	Journal article
Foilsithe / Cruthaithe:	1994

Míreanna comhchosúla

Assignment of the dystonia-parkinsonism syndrome locus, DYT3, to a small region within a 1.8-Mb YAC contig of Xq13.1.
de réir: Haberhausen, G, et al.
Foilsithe / Cruthaithe: (1995)

Construction of a YAC contig spanning the Xq13.3 subband.
de réir: Villard, L, et al.
Foilsithe / Cruthaithe: (1995)

DELINEATION OF THE X-CHROMOSOMAL DYSTONIA-PARKINSONISM (XDP) SYNDROME LOCUS, DYT3, WITHIN YAC AND COSMID CONTIGS OF XQ13.1 AND ISOLATION OF CANDIDATE GENES
de réir: Muller, U, et al.
Foilsithe / Cruthaithe: (1995)

Fine mapping of the human SCIDX1 locus at Xq12-13.1.
de réir: Markiewicz, S, et al.
Foilsithe / Cruthaithe: (1993)

2.6 Mb YAC contig of the human X inactivation center region in Xq13: physical linkage of the RPS4X, PHKA1, XIST and DXS128E genes.
de réir: Lafrenière, R, et al.
Foilsithe / Cruthaithe: (1993)

A 2.6-MB YAC CONTIG OF THE HUMAN X-INACTIVATION CENTER REGION IN XQ13 - PHYSICAL LINKAGE OF THE RPS4X, PHKA1, XIST, AND DXS128E GENES AND REFINEMENT OF THE XIC-CONTAINING INTERVAL
de réir: Lafreniere, R, et al.
Foilsithe / Cruthaithe: (1993)

A 2.8 Mb YAC contig in 11q12-q13 localizes candidate genes for atopy: Fc epsilon RI beta and CD20.
de réir: Stafford, A, et al.
Foilsithe / Cruthaithe: (1994)

HUMAN XP21-YAC CONTIG MAPS
de réir: Walker, A, et al.
Foilsithe / Cruthaithe: (1991)

A contig of non-chimaeric YACs containing the spinal muscular atrophy gene in 5q13.
de réir: Francis, M, et al.
Foilsithe / Cruthaithe: (1993)

Assignment of genes encoding GABAA receptor subunits alpha 1, alpha 6, beta 2, and gamma 2 to a YAC contig of 5q33.
de réir: Kostrzewa, M, et al.
Foilsithe / Cruthaithe: (1996)

CHARACTERIZATION OF MOLECULAR DNA REARRANGEMENTS, WITHIN THE XQ12-]Q13.1 REGION, IN 4 PATIENTS WITH X-LINKED HYPOHIDROTIC ECTODERMAL DYSPLASIA (EDA)
de réir: Thomas, N, et al.
Foilsithe / Cruthaithe: (1993)

Characterization of a 1.0 Mb YAC contig spanning two chromosome breakpoints related to Menkes disease.
de réir: Tümer, Z, et al.
Foilsithe / Cruthaithe: (1992)

CREATING YAC CONTIGS CORRESPONDING TO THE HUMAN DNA FRAGMENTS PRESENT IN IRRADIATION HYBRID CELL-LINES - A YAC CONTIG PHYSICALLY LINKING ZFX AND POLA
de réir: Francis, F, et al.
Foilsithe / Cruthaithe: (1993)

X-LINKED HYPOHIDROTIC ECTODERMAL DYSPLASIA (EDA) - ANALYSIS OF CYTOGENETIC REARRANGEMENTS IN 4 PATIENTS AND DEVELOPMENT OF A DETAILED PHYSICAL MAP WITHIN XQ12-Q13.1.
de réir: Thomas, N, et al.
Foilsithe / Cruthaithe: (1993)

T-Cell Lymphopenia Detected by Newborn Screening in Two Siblings with an Xq13.1 Duplication
de réir: Xavier Rios, et al.
Foilsithe / Cruthaithe: (2017-07-01)

YAC CONTIGS AND PHYSICAL MAPPING OF XP11.23-]P11.22
de réir: Fisher, S, et al.
Foilsithe / Cruthaithe: (1994)

Dinucleotide repeat polymorphisms from DXS106 and DXS227 YACs using a two stage approach.
de réir: Fairweather, N, et al.
Foilsithe / Cruthaithe: (1993)

A YAC contig in Xp21 containing the adrenal hypoplasia congenita and glycerol kinase deficiency genes.
de réir: Walker, A, et al.
Foilsithe / Cruthaithe: (1992)

YAC clone contigs surrounding the Zfx and Pola loci on the mouse X chromosome.
de réir: Hamvas, R, et al.
Foilsithe / Cruthaithe: (1993)

Physical mapping in a YAC contig of 11 markers on the human X chromosome in Xp11.23.
de réir: Hagemann, T, et al.
Foilsithe / Cruthaithe: (1994)

Physical mapping and YAC contig analysis of the region surrounding Xist on the mouse X chromosome.
de réir: Heard, E, et al.
Foilsithe / Cruthaithe: (1993)

A YAC CONTIG ACROSS THE FRAGILE-X REGION DERIVED FROM CHROMOSOME MICRODISSECTION MARKERS
de réir: Hirst, M, et al.
Foilsithe / Cruthaithe: (1991)

Assignment of the gene (EPLG2) encoding a high-affinity binding protein for the receptor tyrosine kinase elk to a 200-kilobasepair region in human chromosome Xq12.
de réir: Fletcher, F, et al.
Foilsithe / Cruthaithe: (1995)

Xq12q13.2 duplication detected in a child in selective exome screening
de réir: A. A. Dokshukina, et al.
Foilsithe / Cruthaithe: (2024-09-01)

Construction of a YAC contig and an STS map spanning 3.6 megabase pairs in Xp22.1.
de réir: Trump, D, et al.
Foilsithe / Cruthaithe: (1996)

XIST IS NOT REQUIRED FOR THE MAINTENANCE OF X-INACTIVATION - ANALYSIS OF THE X-CHROMOSOME BREAKPOINT REGION AT XQ13 IN PATIENTS WITH ACQUIRED ISODICENTRIC X-CHROMOSOME ASSOCIATED WITH LEUKEMIA
de réir: Rider, S, et al.
Foilsithe / Cruthaithe: (1993)

Three genes that escape X chromosome inactivation are clustered within a 6 Mb YAC contig and STS map in Xp11.21-p11.22.
de réir: Miller, A, et al.
Foilsithe / Cruthaithe: (1995)

Detailed physical analysis of a 1.5-megabase YAC contig containing the MXI1 and ADRA2A genes.
de réir: Manca, A, et al.
Foilsithe / Cruthaithe: (1997)

DEFINITION OF THE PHYSICAL AND GENETIC LIMITS OF THE HUNTINGTONS-DISEASE GENE CANDIDATE REGION AND PROGRESS TOWARDS ITS ISOLATION AS A YAC CONTIG
de réir: Bates, G, et al.
Foilsithe / Cruthaithe: (1991)

Genetic analysis of the epidermal differentiation complex (EDC) on human chromosome 1q21: chromosomal orientation, new markers, and a 6-Mb YAC contig.
de réir: Marenholz, I, et al.
Foilsithe / Cruthaithe: (1996)

ISOLATION OF GENES FROM A 1.7-MB YAC CONTIG WITHIN THE ESSENTIAL REGION OF X-LINKED EYE DISORDERS
de réir: Nemeth, A, et al.
Foilsithe / Cruthaithe: (1993)

Turner Syndrome with Isochromosome Xq and Familial Reciprocal Translocation t(4;16)(p15.2;p13.1)
de réir: Cetin Z, et al.
Foilsithe / Cruthaithe: (2011-01-01)

A 2-Mb YAC contig encompassing three loci (DXF34, DXS14, and DXS390) that lie between Xp11.2 translocation breakpoints associated with incontinentia pigmenti type 1.
de réir: Reed, V, et al.
Foilsithe / Cruthaithe: (1994)

Characterization of a highly complex region in Xq13 and mapping of three isodicentric breakpoints associated with preleukemia.
de réir: McDonell, N, et al.
Foilsithe / Cruthaithe: (2000)

MHC class I gene organization in > 1.5-Mb YAC contigs from the H2-M region.
de réir: Jones, E, et al.
Foilsithe / Cruthaithe: (1995)

PHYSICAL AND GENETIC-MAPPING AND POSITIONAL CLONING OF DISEASE GENES IN XCEN-]Q21
de réir: Chelly, J, et al.
Foilsithe / Cruthaithe: (1993)

Isolation of new probes from Xq12-->q13: an example of the screening of reference libraries with Alu-PCR products from radiation hybrids.
de réir: Muscatelli, F, et al.
Foilsithe / Cruthaithe: (1992)

A New Case of 13q12.2q13.1 Microdeletion Syndrome Contributes to Phenotype Delineation
de réir: Giorgia Mandrile, et al.
Foilsithe / Cruthaithe: (2014-01-01)

Construction of two YAC contigs in human Xp11.23-p11.22, one encompassing the loci OATL1, GATA, TFE3, and SYP, the other linking DXS255 to DXS146.
de réir: Fisher, S, et al.
Foilsithe / Cruthaithe: (1995)

High-resolution YAC fragmentation map of 1q21.
de réir: Lioumi, M, et al.
Foilsithe / Cruthaithe: (1998)