Literature DB >> 8012397

The gene for achondroplasia maps to the telomeric region of chromosome 4p.

M Velinov1, S A Slaugenhaupt, I Stoilov, C I Scott, J F Gusella, P Tsipouras.   

Abstract

Achondroplasia is the most common type of genetic dwarfism. It is characterized by disproportionate short stature and other skeletal anomalies resulting from a defect in the maturation of the chondrocytes in the growth plate of the cartilage. We have now mapped the achondroplasia gene near the telomere of the short arm of chromosome 4 (4p16.3), by family linkage studies using 14 pedigrees. A positive lod score of z = 3.35 with no recombinants was obtained with an intragenic marker for IDUA. This localization will facilitate the positional cloning of the disease gene.

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Year:  1994        PMID: 8012397     DOI: 10.1038/ng0394-314

Source DB:  PubMed          Journal:  Nat Genet        ISSN: 1061-4036            Impact factor:   38.330


  18 in total

Review 1.  Advances in Skeletal Dysplasia Genetics.

Authors:  Krista A Geister; Sally A Camper
Journal:  Annu Rev Genomics Hum Genet       Date:  2015-04-22       Impact factor: 8.929

2.  2016 William Allan Award: Human Disease Research: Genetic Cycling and Re-cycling.

Authors:  James F Gusella
Journal:  Am J Hum Genet       Date:  2017-03-02       Impact factor: 11.025

Review 3.  Achondroplasia: Development, pathogenesis, and therapy.

Authors:  David M Ornitz; Laurence Legeai-Mallet
Journal:  Dev Dyn       Date:  2017-03-02       Impact factor: 3.780

4.  In vitro proliferation of achondroplastic and normal mouse chondrocytes, before and after basic fibroblast growth factor stimulation.

Authors:  G Argentin; R Cicchetti
Journal:  Cell Prolif       Date:  2000-12       Impact factor: 6.831

5.  Clinical and genetic heterogeneity of hypochondroplasia.

Authors:  F Rousseau; J Bonaventure; L Legeai-Mallet; H Schmidt; J Weissenbach; P Maroteaux; A Munnich; M Le Merrer
Journal:  J Med Genet       Date:  1996-09       Impact factor: 6.318

6.  Possible genetic heterogeneity in hypochondroplasia.

Authors:  I Stoilov; M W Kilpatrick; P Tsipouras; T Costa
Journal:  J Med Genet       Date:  1995-06       Impact factor: 6.318

7.  Mutations of the fibroblast growth factor receptor-3 gene in one familial and six sporadic cases of achondroplasia in Japanese patients.

Authors:  S Ikegawa; Y Fukushima; M Isomura; F Takada; Y Nakamura
Journal:  Hum Genet       Date:  1995-09       Impact factor: 4.132

8.  A glycine 375-to-cysteine substitution in the transmembrane domain of the fibroblast growth factor receptor-3 in a newborn with achondroplasia.

Authors:  A Superti-Furga; G Eich; H U Bucher; J Wisser; A Giedion; R Gitzelmann; B Steinmann
Journal:  Eur J Pediatr       Date:  1995-03       Impact factor: 3.183

9.  How reliable are standard radiographic measures of the foot and ankle in children with achondroplasia?

Authors:  Jia Xu; Kwang-Won Park; Qing-Lin Kang; Young-Jin Jung; Hae-Ryong Song
Journal:  Clin Orthop Relat Res       Date:  2013-04-23       Impact factor: 4.176

10.  Molecular studies of achondroplasia.

Authors:  Risha Nahar; Renu Saxena; Sudha Kohli; Ratna Puri; Ishwar Chandra Verma
Journal:  Indian J Orthop       Date:  2009-04       Impact factor: 1.251

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