Literature DB >> 8322806

Inverted insertion of chromosome 7q and ectrodactyly.

K Naritomi1, Y Izumikawa, T Tohma, K Hirayama.   

Abstract

An inverted insertion of a segment 7q22-q34 into 3q21 was found in a mentally normal male infant with ectrodactyly of a hand and the feet. A putative gene for ectrodactyly seems to be assigned at 7q22.

Entities:  

Mesh：

Year:  1993        PMID： 8322806     DOI： 10.1002/ajmg.1320460505

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


  10 in total

1.  Refined mapping of a gene for split hand-split foot malformation (SHFM3) on chromosome 10q25.

Authors:  A Raas-Rothschild; S Manouvrier; M Gonzales; J P Farriaux; S Lyonnet; A Munnich
Journal:  J Med Genet       Date:  1996-12       Impact factor: 6.318

2.  Split Hand/Foot Malformation Associated with 7q21.3 Microdeletion: A Case Report.

Authors:  Aswini Sivasankaran; Ambika Srikanth; Pooja S Kulshreshtha; Deenadayalu Anuradha; Jayarama S Kadandale; Chandra R Samuel
Journal:  Mol Syndromol       Date:  2016-02-03

3.  Bilateral split hand/foot malformation and inv(7)(p22q21.3).

Authors:  J M Cobben; J B Verheij; W H Eisma; P H Robinson; R P Zwierstra; B Leegte; S Castedo
Journal:  J Med Genet       Date:  1995-05       Impact factor: 6.318

Review 4.  Cleft hand/foot: clinical and developmental aspects.

Authors:  P W Buss
Journal:  J Med Genet       Date:  1994-09       Impact factor: 6.318

5.  Evidence for locus heterogeneity in human autosomal dominant split hand/split foot malformation.

Authors:  S E Palmer; S W Scherer; M Kukolich; E M Wijsman; L C Tsui; K Stephens; J P Evans
Journal:  Am J Hum Genet       Date:  1994-07       Impact factor: 11.025

6.  The phenotypic effects of chromosome rearrangement involving bands 7q21.3 and 22q13.3.

Authors:  A Slavotinek; E Maher; P Gregory; P Rowlandson; S M Huson
Journal:  J Med Genet       Date:  1997-10       Impact factor: 6.318

7.  Split hand/split foot malformation, deafness, and mental retardation with a complex cytogenetic rearrangement involving 7q21.3.

Authors:  J Ignatius; S Knuutila; S W Scherer; B Trask; J Kere
Journal:  J Med Genet       Date:  1996-06       Impact factor: 6.318

Review 8.  Fine mapping of the autosomal dominant split hand/split foot locus on chromosome 7, band q21.3-q22.1.

Authors:  S W Scherer; P Poorkaj; T Allen; J Kim; D Geshuri; M Nunes; S Soder; K Stephens; R A Pagon; M A Patton
Journal:  Am J Hum Genet       Date:  1994-07       Impact factor: 11.025

9.  Phenotypic subregions within the split-hand/foot malformation 1 locus.

Authors:  Malene B Rasmussen; Sven Kreiborg; Per Jensen; Mads Bak; Yuan Mang; Marianne Lodahl; Esben Budtz-Jørgensen; Niels Tommerup; Lisbeth Tranebjærg; Nanna D Rendtorff
Journal:  Hum Genet       Date:  2016-02-02       Impact factor: 4.132

Review 10.  Split hand/foot malformation genetics supports the chromosome 7 copy segregation mechanism for human limb development.

Authors:  Amar J S Klar
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2016-12-19       Impact factor: 6.237
  10 in total

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