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.

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.

We demonstrate that all the repeat elements representing the conserved loci DXF34 and DXS390 lie between the X;9 and the X;17 translocation breakpoints associated with incontinentia pigmenti type 1 (IP1). Sequence-tagged sites (STSs) at DXF34S1, DXS14, and DXS390 have been used to isolate YAC clones...

Descripció completa

Dades bibliogràfiques
Autors principals:	Reed, V, Rider, S, Maslen, G, Hatchwell, E, Blair, H, Uwechue, I, Craig, I, Laval, S, Monaco, A, Boyd, Y
Format:	Journal article
Idioma:	English
Publicat:	1994

Ítems similars

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.
per: Fisher, S, et al.
Publicat: (1995)

Dinucleotide repeat polymorphisms from DXS106 and DXS227 YACs using a two stage approach.
per: Fairweather, N, et al.
Publicat: (1993)

Primers for the dinucleotide repeat at the DXS453 locus also recognizes the DXS983 locus.
per: Rider, S, et al.
Publicat: (1993)

PRIMERS FOR THE DINUCLEOTIDE REPEAT AT THE DXS453 LOCUS ALSO RECOGNIZES THE DXS983 LOCUS
per: Rider, S, et al.
Publicat: (1993)

HUMAN XP21-YAC CONTIG MAPS
per: Walker, A, et al.
Publicat: (1991)

YAC CONTIGS AND PHYSICAL MAPPING OF XP11.23-]P11.22
per: Fisher, S, et al.
Publicat: (1994)

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

DXS106 AND DXS559 FLANK THE X-LINKED DYSTONIA-PARKINSONISM LOCUS, DYT3
per: Wagner, T, et al.
Publicat: (1994)

Linkage analysis of two cloned DNA sequences, DXS197 and DXS207, in hypophosphatemic rickets families.
per: Thakker, R, et al.
Publicat: (1990)

DXS106 and DXS559 flank the X-linked dystonia-parkinsonism syndrome locus (DYT3).
per: Müller, U, et al.
Publicat: (1994)

Incontinentia Pigmenti
per: Cengiz Yalçınkaya, et al.
Publicat: (2007-10-01)

Incontinentia pigmenti
per: Claudia Schermann Poziomczyk, et al.
Publicat: (2014-01-01)

Incontinentia pigmenti
per: Hegde Sundeep, et al.
Publicat: (2006-05-01)

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
per: Lafreniere, R, et al.
Publicat: (1993)

Retinopathy in incontinentia pigmenti
per: Pukhraj Rishi, et al.
Publicat: (2019-01-01)

LINKAGE ANALYSIS OF 3 CLONED DNA-SEQUENCES, DXS294, CDR AND DXS105, IN X-LINKED RECESSIVE HYPOPARATHYROID FAMILIES
per: Thakker, R, et al.
Publicat: (1991)

Genetic analysis of DXS101and DXS6807 short tandem repeat (X-STR) in samples of Iraqi Arab male population
per: Hayder Allawi Khaleefah, et al.
Publicat: (2020-12-01)

Isolation of DNTR polymorphisms from yeast artificial chromosomes encompassing X chromosomal loci PGK1 and DXS56.
per: Graeber, M, et al.
Publicat: (1992)

YAC CONTIGS IN XQ12-]Q13.1
per: Rider, S, et al.
Publicat: (1994)

The evolution of radio sources in the UKIDSS-DXS-XMM-LSS field
per: McAlpine, K, et al.
Publicat: (2011)

Incontinentia pigmenti with neurologic and oculodental disorders
per: Jorge Arturo Avina Fierro, et al.
Publicat: (2016-01-01)

Two male patients with incontinentia pigmenti
per: Minić Snežana, et al.
Publicat: (2010-01-01)

A YAC contig in Xp21 containing the adrenal hypoplasia congenita and glycerol kinase deficiency genes.
per: Walker, A, et al.
Publicat: (1992)

Physical mapping in a YAC contig of 11 markers on the human X chromosome in Xp11.23.
per: Hagemann, T, et al.
Publicat: (1994)

Characterization of a 1.0 Mb YAC contig spanning two chromosome breakpoints related to Menkes disease.
per: Tümer, Z, et al.
Publicat: (1992)

The discovery of a massive supercluster at z=0.9 in the UKIDSS DXS
per: Swinbank, A, et al.
Publicat: (2007)

Construction of a YAC contig and an STS map spanning 3.6 megabase pairs in Xp22.1.
per: Trump, D, et al.
Publicat: (1996)

Cephalometric skeletal evaluation of patients with Incontinentia Pigmenti
per: Marcia Angelica Peter Maahs, et al.
Publicat: (2014-05-01)

Case report: A case of incontinentia pigmenti
per: Lingfeng Xie, et al.
Publicat: (2023-05-01)

Retinal Neovascularization in Two Patients with Incontinentia Pigmenti
per: Dwiyana RF, et al.
Publicat: (2022-04-01)

Sporadic case of incontinentia pigmenti in identical twins
per: Shekhar Neema, et al.
Publicat: (2017-01-01)

Dermatoscopy in the Diagnostics of Incontinentia Pigmenti Skin Lesions
per: Snezana Minic, et al.
Publicat: (2022-07-01)

Layer by layer encapsulation of PRM/DXS/neutravidin and antibody on calcium carbonate core
per: Liaw, Zi Yen.
Publicat: (2009)

Identification of Inhibitors of the Anti-Infective Target DXS Using Dynamic Combinatorial Chemistry
per: Ravindra P. Jumde, et al.
Publicat: (2019-08-01)

Dent's disease, a renal Fanconi syndrome with nephrocalcinosis and kidney stones, is associated with a microdeletion involving DXS255 and maps to Xp11.22.
per: Pook, M, et al.
Publicat: (1993)

Uncovering incontinentia pigmenti: From DNA sequence to pathophysiology
per: Kang, Nien How, et al.
Publicat: (2022)

Incontinentia Pigmenti in a Newborn. A Case Report
per: Yahiris García Rodríguez, et al.
Publicat: (2015-09-01)

Incontinentia Pigmenti-Dermoscopy Features of Early Evolving Disease
per: M Vijaikumar, et al.
Publicat: (2025-01-01)

Incontinentia pigmenti with cleft palate: A case report
per: Ningning hu, et al.
Publicat: (2025-01-01)

Incontinentia pigmenti: a case report and literature review
per: Sinan Emre, et al.
Publicat: (2009-04-01)