MAPPING OF THE X-LINKED IDIOPATHIC HYPOPARATHYROID GENE TO XQ26-XQ27 BY LINKAGE STUDIES

MAPPING OF THE X-LINKED IDIOPATHIC HYPOPARATHYROID GENE TO XQ26-XQ27 BY LINKAGE STUDIES

التفاصيل البيبلوغرافية
المؤلفون الرئيسيون:	Thakker, R, Davies, K, Whyte, M, Wooding, C, Oriordan, J
التنسيق:	Journal article
منشور في:	1989

مواد مشابهة

Mapping the gene causing X-linked recessive idiopathic hypoparathyroidism to Xq26-Xq27 by linkage studies.
حسب: Thakker, R, وآخرون
منشور في: (1990)

Localisation of X linked recessive idiopathic hypoparathyroidism to a 1.5 Mb region on Xq26-q27.
حسب: Trump, D, وآخرون
منشور في: (1998)

Genetic mapping studies of the X-linked recessive hypoparathyroid gene on the X chromosome (Xq27).
حسب: Dixon, P, وآخرون
منشور في: (1996)

Physical map of the Xq27 candidate region for X-linked recessive hypoparathyroidism in two kindreds merged by mitochondrial DNA analysis
حسب: Mumm, S, وآخرون
منشور في: (1996)

X-linked recessive hypoparathyroidism is caused by a molecular deletional-insertion involving chromosomes Xq27 and 2p25.
حسب: Bowl, MR, وآخرون
منشور في: (2001)

X-linked hypoparathyroidism region on Xq27 is evolutionarily conserved with regions on 3q26 and 13q34 and contains a novel P-type ATPase.
حسب: Andrew Nesbit, M, وآخرون
منشور في: (2004)

An interstitial deletion-insertion involving chromosomes 2p25.3 and Xq27.1, near SOX3, causes X-linked recessive hypoparathyroidism.
حسب: Bowl, MR, وآخرون
منشور في: (2005)

Distal Xq duplication and functional Xq disomy
حسب: Schluth-Bolard Caroline, وآخرون
منشور في: (2009-02-01)

A LINKAGE STUDY USING DNA MARKERS LOCALIZES THE GENE FOR X-LINKED DOMINANT CHARCOT-MARIE-TOOTH DISEASE AT XQ13-XQ22
حسب: Beckett, J, وآخرون
منشور في: (1985)

Recurrent Microdeletions at Xq27.3-Xq28 and Male Infertility: A Study in the Czech Population.
حسب: Blanka Chylíková, وآخرون
منشور في: (2016-01-01)

Analysis of Xq27-28 linkage in the international consortium for prostate cancer genetics (ICPCG) families
حسب: Bailey-Wilson Joan E, وآخرون
منشور في: (2012-06-01)

LINKAGE ANALYSIS OF 3 CLONED DNA-SEQUENCES, DXS294, CDR AND DXS105, IN X-LINKED RECESSIVE HYPOPARATHYROID FAMILIES
حسب: Thakker, R, وآخرون
منشور في: (1991)

PPM-X: a new X-linked mental retardation syndrome with psychosis, pyramidal signs, and macroorchidism maps to Xq28.
حسب: Lindsay, S, وآخرون
منشور في: (1996)

Identification and Characterization of Nine Novel X-Chromosomal Short Tandem Repeats on Xp21.1, Xq21.31, and Xq23 Regions
حسب: Qinrui Yang, وآخرون
منشور في: (2021-11-01)

ChrXq27.3 miRNA cluster functions in cancer development
حسب: Kosuke Yoshida, وآخرون
منشور في: (2021-03-01)

X-linked alpha-thalassemia/mental retardation (ATR-X) syndrome: localization to Xq12-q21.31 by X inactivation and linkage analysis.
حسب: Gibbons, R, وآخرون
منشور في: (1992)

Two Patients with X Chromosome Duplication: dupXp and dupXq
حسب: Ozer O, وآخرون
منشور في: (2009-01-01)

Incidental detection of partial Xq deletion (Xq21→qter), or 46,X,del(X)(q21) in a 17-year-old girl with irregular menstrual cycle
حسب: Chih-Ping Chen
منشور في: (2023-11-01)

YAC CONTIGS IN XQ12-]Q13.1
حسب: Rider, S, وآخرون
منشور في: (1994)

Linear order of new and established DNA markers around the fragile site at Xq27.3.
حسب: Hirst, M, وآخرون
منشور في: (1991)

Fine mapping of the human SCIDX1 locus at Xq12-13.1.
حسب: Markiewicz, S, وآخرون
منشور في: (1993)

A Case With Short Stature, Growth Hormone Deficiency and 46, XX, Xq27-qter Deletion
حسب: Şule Yıldırım, وآخرون
منشور في: (2017-12-01)

Characterization of novel isoforms and evaluation of <it>SNF2L/SMARCA1 </it>as a candidate gene for X-linked mental retardation in 12 families linked to Xq25-26
حسب: Lavigne Paul, وآخرون
منشور في: (2008-02-01)

2.6 Mb YAC contig of the human X inactivation center region in Xq13: physical linkage of the RPS4X, PHKA1, XIST and DXS128E genes.
حسب: Lafrenière, R, وآخرون
منشور في: (1993)

B CELL DEFECTS IN A PATIENT WITH XQ24 DELETION
حسب: Anzilotti, C, وآخرون
منشور في: (2012)

Systemic lupus erythematosus: genetic variants in Xq28 region
حسب: Noha Doudar, وآخرون
منشور في: (2019-10-01)

The systematic functional characterisation of Xq28 genes prioritises candidate disease genes
حسب: Wiemann Stefan, وآخرون
منشور في: (2006-02-01)

Optical Genome Mapping Identifies a Second Xq27.1 Rearrangement Associated With Charcot–Marie–Tooth Neuropathy CMTX3
حسب: Elisa Rahikkala, وآخرون
منشور في: (2024-09-01)

Construction of a YAC contig spanning the Xq13.3 subband.
حسب: Villard, L, وآخرون
منشور في: (1995)

New candidate genes for X-linked recessive hypoparathyroidism.
حسب: Mumm, S, وآخرون
منشور في: (1999)

Germline intergenic duplications at Xq26.1 underlie Bazex-Dupré-Christol basal cell carcinoma susceptibility syndrome
حسب: Liu, Yanshan, وآخرون
منشور في: (2022)

Molecular cytogenetic characterization of Xp22.32→pter deletion and Xq26.3→qter duplication in a male fetus associated with 46,Y,rec(X)dup(Xq) inv(X)(p22.3q26.3), a hypoplastic left heart, short stature, and maternal X chromosome pericentric inversion
حسب: Chih-Ping Chen, وآخرون
منشور في: (2016-10-01)

Population genetics of the FRAXE and FRAXF GCC repeats, and a novel CGG repeat, in Xq28.
حسب: Ritchie, R, وآخرون
منشور في: (1997)

Prenatal diagnosis of familial 46,X,del(X)(q27.1) with an Xq27.1-q28 deletion and an Xp22.33 microduplication in an asymptomatic mother carrier
حسب: Chih-Ping Chen
منشور في: (2025-03-01)

Characterization of a highly complex region in Xq13 and mapping of three isodicentric breakpoints associated with preleukemia.
حسب: McDonell, N, وآخرون
منشور في: (2000)

SHOX Duplication and Tall Stature in a Patient with Xq Deletion and Vascular Disease
حسب: J. M. Ramirez, وآخرون
منشور في: (2019-01-01)

X-LINKED HYPOHIDROTIC ECTODERMAL DYSPLASIA (EDA) - ANALYSIS OF CYTOGENETIC REARRANGEMENTS IN 4 PATIENTS AND DEVELOPMENT OF A DETAILED PHYSICAL MAP WITHIN XQ12-Q13.1.
حسب: Thomas, N, وآخرون
منشور في: (1993)

CHARACTERIZATION OF MOLECULAR DNA REARRANGEMENTS, WITHIN THE XQ12-]Q13.1 REGION, IN 4 PATIENTS WITH X-LINKED HYPOHIDROTIC ECTODERMAL DYSPLASIA (EDA)
حسب: Thomas, N, وآخرون
منشور في: (1993)

Identification of a De Novo Xq26.2 Microduplication Encompassing <i>FIRRE</i> Gene in a Child with Intellectual Disability
حسب: Gianmaria Miolo, وآخرون
منشور في: (2020-11-01)

Isolation of the human chromosomal band Xq28 within somatic cell hybrids by fragile X site breakage.
حسب: Warren, S, وآخرون
منشور في: (1990)