Genetic and physical mapping on chromosome 4 narrows the localization of the gene for facioscapulohumeral muscular dystrophy (FSHD) (scientific article published on August 1, 1992)

Prenatal identification of a girl with a t(X;4)(p21;q35) translocation: molecular characterisation, paternal origin, and association with muscular dystrophy

Q33597984

Variable number of tandem repeat (VNTR) markers for human gene mapping

Q34163031

Factor XI gene (F11) is located on the distal end of the long arm of human chromosome 4.

Q34482812

Report of the committee on linkage and gene order

Q34546618

Linkage localization of facioscapulohumeral muscular dystrophy (FSHD) in 4q35

Q35195701

Regional mapping of facioscapulohumeral muscular dystrophy gene on 4q35: combined analysis of an international consortium

Q35195748

Isolation and mapping of a polymorphic DNA sequence pH30 on chromosome 4[HGM provisional no. D4S139]

Q35229005

Pairwise linkage analysis of 11 loci on human chromosome 4.

Q35245357

Abundant class of human DNA polymorphisms which can be typed using the polymerase chain reaction

Q35247229

Multipoint linkage analysis in neurofibromatosis type I: an international collaboration

Q35247369

Localization of the genetic defect in familial adenomatous polyposis within a small region of chromosome 5

Q35247824

Molecular analysis of X-autosome translocations in females with Duchenne muscular dystrophy

Q35936077

Genetic analysis of indefinite division in human cells: evidence for a cell senescence-related gene(s) on human chromosome 4.

Q37540466

Report of the committee on the genetic constitution of chromosome 4.

Q38695664

Cloning of the Duchenne/Becker muscular dystrophy locus

Q39539162

Dinucleotide repeat polymorphism at the D4S174 locus

Q40519313

Isolation and characterization of a hypervariable region [D4S163] on chromosome 4.

Q40530553

A highly polymorphic VNTR locus on the long arm of chromosome 4

Q40532107

Centre d'etude du polymorphisme humain (CEPH): collaborative genetic mapping of the human genome

Q43559819

DNA sequence polymorphisms in Alu repeats

Q44137040

Recombination events suggest potential sites for the Huntington's disease gene

Q44168431

P433

issue

P407

language of work or name

English

Q1860

P921

main subject

human chromosome 4

Q836605

facioscapulohumeral muscular dystrophy

Q1399182

P304

page(s)

432-439

P577

publication date

1992-08-01

P1433

published in

American Journal of Human Genetics

Q4744249

P1476

title

Genetic and physical mapping on chromosome 4 narrows the localization of the gene for facioscapulohumeral muscular dystrophy (FSHD)

P478

volume

Reverse relations

cites work (P2860)

Q35195000	A radiation hybrid map of 15 loci on the distal long arm of chromosome 4, the region containing the gene responsible for facioscapulohumeral muscular dystrophy (FSHD).
Q56969125	Chromosome 4q35 haplotypes and DNA rearrangements segregating in affected subjects of 19 Italian families with facioscapulohumeral musculatur dystrophy (FSHD)
Q34328093	Comprehensive expression analysis of FSHD candidate genes at the mRNA and protein level
Q71952876	DNA rearrangements in Japanese facioscapulohumeral muscular dystrophy patients: clinical correlations
Q67518183	Framework multipoint map of the long arm of human chromosome 4 and telomeric localization of the gene for FSHD
Q33681314	Identical de novo mutation at the D4F104S1 locus in monozygotic male twins affected by facioscapulohumeral muscular dystrophy (FSHD) with different clinical expression.
Q24623433	International Union of Basic and Clinical Pharmacology. LXXV. Nomenclature, classification, and pharmacology of G protein-coupled melatonin receptors
Q35195701	Linkage localization of facioscapulohumeral muscular dystrophy (FSHD) in 4q35
Q72720052	Linkage mapping of the tumor necrosis factor receptor 2 (TNFR2) gene to 1p36.2 using the single-strand conformation polymorphism technique
Q45292058	Linkage, but not gene order, of homologous loci, including alpha-L-iduronidase (Idua), is conserved in the Huntington disease region of the mouse and human genomes.
Q33677298	Monosomy of distal 4q does not cause facioscapulohumeral muscular dystrophy
Q34329087	New multiplex PCR-based protocol allowing indirect diagnosis of FSHD on single cells: can PGD be offered despite high risk of recombination?
Q46971971	The DNA rearrangement associated with facioscapulohumeral muscular dystrophy involves a heterochromatin-associated repetitive element: implications for a role of chromatin structure in the pathogenesis of the disease.
Q34335333	The human skeletal muscle adenine nucleotide translocator gene maps to chromosome 4q35 in the region of the facioscapulohumeral muscular dystrophy locus
Q35029933	The incidence of mini- and micro-satellite repetitive DNA in the canine genome
Q35195712	The mapping of chromosome 4q markers in relation to facioscapulohumeral muscular dystrophy (FSHD)

P953	full work available at URL	https://europepmc.org/articles/PMC1682692
		https://europepmc.org/articles/PMC1682692?pdf=render
		https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/1642243/?tool=EBI
		https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/1642243/pdf/?tool=EBI
P932	PMC publication ID	1682692
P698	PubMed publication ID	1642243