Literature DB >> 3074733

A computer program to make linkage analysis with LIPED and LINKAGE easier to perform and less prone to input errors.

J Attwood1, S Bryant.   

Abstract

Mesh：

Year:  1988        PMID： 3074733     DOI： 10.1111/j.1469-1809.1988.tb01103.x

Source DB:  PubMed          Journal:  Ann Hum Genet        ISSN： 0003-4800            Impact factor:   1.670


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  28 in total

1.  Clinical and molecular genetic characterisation of a family segregating autosomal dominant retinitis pigmentosa and sensorineural deafness.

Authors:  P Kenna; F Mansergh; S Millington-Ward; A Erven; R Kumar-Singh; R Brennan; G J Farrar; P Humphries
Journal:  Br J Ophthalmol       Date:  1997-03       Impact factor: 4.638

2.  Connexin46 mutations in autosomal dominant congenital cataract.

Authors:  D Mackay; A Ionides; Z Kibar; G Rouleau; V Berry; A Moore; A Shiels; S Bhattacharya
Journal:  Am J Hum Genet       Date:  1999-05       Impact factor: 11.025

3.  Linkage to D3S47 (C17) in one large autosomal dominant retinitis pigmentosa family and exclusion in another: confirmation of genetic heterogeneity.

Authors:  D H Lester; C F Inglehearn; R Bashir; H Ackford; L Esakowitz; M Jay; A C Bird; A F Wright; S S Papiha; S S Bhattacharya
Journal:  Am J Hum Genet       Date:  1990-09       Impact factor: 11.025

4.  Application of intragenic DNA probes in prenatal screening for retinoblastoma gene carriers in the United Kingdom.

Authors:  Z O Onadim; C D Mitchell; P C Rutland; B G Buckle; M Jay; J L Hungerford; K Harper; J K Cowell
Journal:  Arch Dis Child       Date:  1990-07       Impact factor: 3.791

Review 5.  Software for genetic linkage analysis: an update.

Authors:  S P Bryant
Journal:  Mol Biotechnol       Date:  1996-02       Impact factor: 2.695

6.  A new family of Greek origin maps to the CRD locus for autosomal dominant cone-rod dystrophy on 19q.

Authors:  M Papaioannou; D Bessant; A Payne; J Bellingham; C Rougas; A Loutradis-Anagnostou; C Gregory-Evans; A Balassopoulou; S Bhattacharya
Journal:  J Med Genet       Date:  1998-05       Impact factor: 6.318

7.  Familial glaucoma iridogoniodysplasia maps to a 6p25 region implicated in primary congenital glaucoma and iridogoniodysgenesis anomaly.

Authors:  T Jordan; N Ebenezer; R Manners; J McGill; S Bhattacharya
Journal:  Am J Hum Genet       Date:  1997-10       Impact factor: 11.025

8.  Genetic refinement of dominant optic atrophy (OPA1) locus to within a 2 cM interval of chromosome 3q.

Authors:  M Votruba; A T Moore; S S Bhattacharya
Journal:  J Med Genet       Date:  1997-02       Impact factor: 6.318

9.  Linkage of PGK1 to X-linked severe combined immunodeficiency (IMD4) allows predictive testing in families with no surviving male.

Authors:  J Goodship; R Levinsky; S Malcolm
Journal:  Hum Genet       Date:  1989-12       Impact factor: 4.132

10.  Exclusion of the APC gene as the cause of a variant form of familial adenomatous polyposis (FAP)

Authors:  A Stella; N Resta; M Gentile; F Susca; C Mareni; M P Montera; G Guanti
Journal:  Am J Hum Genet       Date:  1993-11       Impact factor: 11.025
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