Literature DB >> 8411023

Psychosocial genetics: an emerging scientific discipline.

P S Harper.   

Abstract

Mesh：

Year:  1993        PMID： 8411023      PMCID： PMC1016450          DOI： 10.1136/jmg.30.7.537

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


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  25 in total

1.  A three-base-pair deletion in the peripherin-RDS gene in one form of retinitis pigmentosa.

Authors:  G J Farrar; P Kenna; S A Jordan; R Kumar-Singh; M M Humphries; E M Sharp; D M Sheils; P Humphries
Journal:  Nature       Date:  1991-12-12       Impact factor: 49.962

2.  Autosomal dominantly inherited macular dystrophy with preferential short-wavelength sensitive cone involvement.

Authors:  G H Bresnick; V C Smith; J Pokorny
Journal:  Am J Ophthalmol       Date:  1989-09-15       Impact factor: 5.258

3.  Molecular genetics of inherited variation in human color vision.

Authors:  J Nathans; T P Piantanida; R L Eddy; T B Shows; D S Hogness
Journal:  Science       Date:  1986-04-11       Impact factor: 47.728

4.  Mutations in the human retinal degeneration slow gene in autosomal dominant retinitis pigmentosa.

Authors:  K Kajiwara; L B Hahn; S Mukai; G H Travis; E L Berson; T P Dryja
Journal:  Nature       Date:  1991-12-12       Impact factor: 49.962

5.  Cone dystrophy, nyctalopia, and supernormal rod responses. A new retinal degeneration.

Authors:  P Gouras; H M Eggers; C J MacKay
Journal:  Arch Ophthalmol       Date:  1983-05

6.  A point mutation of the rhodopsin gene in one form of retinitis pigmentosa.

Authors:  T P Dryja; T L McGee; E Reichel; L B Hahn; G S Cowley; D W Yandell; M A Sandberg; E L Berson
Journal:  Nature       Date:  1990-01-25       Impact factor: 49.962

7.  Color plates to help identify patients with blue cone monochromatism.

Authors:  E L Berson; M A Sandberg; B Rosner; P L Sullivan
Journal:  Am J Ophthalmol       Date:  1983-06       Impact factor: 5.258

8.  Rhodopsin mutations in autosomal dominant retinitis pigmentosa.

Authors:  C H Sung; C M Davenport; J C Hennessey; I H Maumenee; S G Jacobson; J R Heckenlively; R Nowakowski; G Fishman; P Gouras; J Nathans
Journal:  Proc Natl Acad Sci U S A       Date:  1991-08-01       Impact factor: 11.205

9.  X-linked recessive cone dystrophy with tapetal-like sheen. A newly recognized entity with Mizuo-Nakamura phenomenon.

Authors:  J R Heckenlively; R G Weleber
Journal:  Arch Ophthalmol       Date:  1986-09

10.  X-linked progressive cone dystrophy. Clinical characteristics of affected males and female carriers.

Authors:  D M Jacobson; H S Thompson; J A Bartley
Journal:  Ophthalmology       Date:  1989-06       Impact factor: 12.079
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  2 in total

1.  The perceived advantages and disadvantages of presymptomatic testing for Machado-Joseph disease: development of a new self-response inventory.

Authors:  Luísa Rolim; José A Zagalo-Cardoso; Constança Paúl; Jorge Sequeiros; Manuela Fleming
Journal:  J Genet Couns       Date:  2006-09-27       Impact factor: 2.537

2.  Proceed with much more caution.

Authors:  J Schmidtke
Journal:  Hum Genet       Date:  1994-07       Impact factor: 4.132
  2 in total

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