Literature DB >> 8825921

Ophthalmic genetics: a genealogical guide to sources in England and Wales.

M Jay1.   

Abstract

Large pedigrees are fundamental to seeking new genes; they can be constructed on the basis of a family history but can frequently be enlarged considerably from public records. Genealogical sources in England and Wales consist of public records such as civil registration of births, marriages, and deaths, census returns, wills, and church records. Details are given as to their use and where they are to be found. In addition, examples are given of how archival material and pathology reports may be used to compile extensive pedigrees which can span 10 generations.

Mesh:

Year:  1995        PMID: 8825921      PMCID: PMC1051774          DOI: 10.1136/jmg.32.12.946

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  19 in total

1.  Nine generations of a family with autosomal dominant retinitis pigmentosa and evidence of variable expressivity from census records.

Authors:  M Jay; A C Bird; A N Moore; B Jay
Journal:  J Med Genet       Date:  1992-12       Impact factor: 6.318

2.  Choroideremia; clinical and genetic aspects.

Authors:  A SORSBY; A FRANCESCHETTI; R JOSEPH; J B DAVEY
Journal:  Br J Ophthalmol       Date:  1952-10       Impact factor: 4.638

3.  Immunogenetics of retinoblastoma.

Authors:  A L Jones
Journal:  Trans Ophthalmol Soc U K       Date:  1974

4.  Retinoblastoma associated with other primary malignant tumours.

Authors:  G Aherne
Journal:  Trans Ophthalmol Soc U K       Date:  1974

5.  Congenital endothelial corneal dystrophy. Clinical, pathological, and genetic study.

Authors:  W G Pearce; R C Tripathi; G Morgan
Journal:  Br J Ophthalmol       Date:  1969-09       Impact factor: 4.638

6.  Progressive bifocal chorio-retinal atrophy. A rare familial disease of the eyes.

Authors:  A A Douglas; I Waheed; C T Wyse
Journal:  Br J Ophthalmol       Date:  1968-10       Impact factor: 4.638

7.  Public records and recognition of genetic disease in Scotland.

Authors:  S Collyer; R De Mey
Journal:  Clin Genet       Date:  1987-03       Impact factor: 4.438

8.  Further refinement of the location for autosomal dominant retinitis pigmentosa on chromosome 7p (RP9).

Authors:  C F Inglehearn; T J Keen; M al-Maghtheh; C Y Gregory; M R Jay; A T Moore; A C Bird; S S Bhattacharya
Journal:  Am J Hum Genet       Date:  1994-04       Impact factor: 11.025

9.  Autosomal dominant retinitis pigmentosa with apparent incomplete penetrance: a clinical, electrophysiological, psychophysical, and molecular genetic study.

Authors:  A T Moore; F Fitzke; M Jay; G B Arden; C F Inglehearn; T J Keen; S S Bhattacharya; A C Bird
Journal:  Br J Ophthalmol       Date:  1993-08       Impact factor: 4.638

10.  Familial malignant melanoma of the uvea and p53: a Victorian detective story.

Authors:  M Jay; A C McCartney
Journal:  Surv Ophthalmol       Date:  1993 May-Jun       Impact factor: 6.048

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  1 in total

1.  Highly consistent genetic alterations in childhood adrenocortical tumours detected by comparative genomic hybridization.

Authors:  L A James; A M Kelsey; J M Birch; J M Varley
Journal:  Br J Cancer       Date:  1999-09       Impact factor: 7.640

  1 in total

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