Literature DB >> 2624254

Linkage localization of Börjeson-Forssman-Lehmann syndrome.

K D Mathews1, H H Ardinger, D Y Nishimura, K H Buetow, J C Murray, J A Bartley.   

Abstract

Börjeson-Forssman-Lehmann syndrome (BFLS) is a form of X-linked mental retardation (XLMR) with characteristic minor physical anomalies. It has no biochemical or cytogenetic markers. Heterozygous females may be entirely normal or may have mild-to-moderate manifestations. We studied 41 individuals from one family with BFLS for linkage on the X chromosome. The highest lod scores were 2.32 with DXS10 and 2.24 with DXS51, both at a theta = 0.0. A single recombinant was found between HPRT and BFLS. These results suggest that the BFLS locus is on the distal portion of Xq. Previously reported linkage studies in families with XLMR have not shown linkage with DXS10. This study suggests that one of the several X chromosome loci whose dysfunction is associated with mental retardation is located on distal Xq.

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Mesh:

Year:  1989        PMID: 2624254     DOI: 10.1002/ajmg.1320340403

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  8 in total

Review 1.  X linked mental retardation.

Authors:  I A Glass
Journal:  J Med Genet       Date:  1991-06       Impact factor: 6.318

2.  X-linked mental retardation: in pursuit of a gene map.

Authors:  C E Schwartz
Journal:  Am J Hum Genet       Date:  1993-06       Impact factor: 11.025

3.  A unique form of mental retardation with a distinctive phenotype maps to Xq26-q27.

Authors:  V Shashi; M N Berry; S Shoaf; J J Sciote; D Goldstein; T C Hart
Journal:  Am J Hum Genet       Date:  2000-02       Impact factor: 11.025

4.  Localisation of a gene for non-specific X linked mental retardation (MRX46) to Xq25-q26.

Authors:  H G Yntema; B C Hamel; A P Smits; T van Roosmalen; B van den Helm; H Kremer; H H Ropers; D F Smeets; H van Bokhoven
Journal:  J Med Genet       Date:  1998-10       Impact factor: 6.318

5.  The PHF6 Mutation c.1A>G; pM1V Causes Börjeson-Forsman-Lehmann Syndrome in a Family with Four Affected Young Boys.

Authors:  Anja Ernst; Vang Q Le; Allan T Højland; Inge S Pedersen; Tine H Sørensen; Lise L Bjerregaard; Troels J B Lyngbye; Ninna M Gammelager; Henrik Krarup; Michael B Petersen
Journal:  Mol Syndromol       Date:  2015-09-29

6.  Synaptophysin: structure of the human gene and assignment to the X chromosome in man and mouse.

Authors:  T Ozçelik; R G Lafreniere; B T Archer; P A Johnston; H F Willard; U Francke; T C Südhof
Journal:  Am J Hum Genet       Date:  1990-09       Impact factor: 11.025

7.  Linkage of the gene for an X-linked mental retardation disorder to a hypervariable (AGAT)n repeat motif within the human hypoxanthine phosphoribosyltransferase (HPRT) locus (Xq26).

Authors:  T H Huang; J F Hejtmancik; A Edwards; A L Pettigrew; C A Herrera; H A Hammond; C T Caskey; H Y Zoghbi; D H Ledbetter
Journal:  Am J Hum Genet       Date:  1991-12       Impact factor: 11.025

Review 8.  PHF6 Degrees of Separation: The Multifaceted Roles of a Chromatin Adaptor Protein.

Authors:  Matthew A M Todd; Danton Ivanochko; David J Picketts
Journal:  Genes (Basel)       Date:  2015-06-19       Impact factor: 4.096

  8 in total

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