Literature DB >> 5307229

Genetic linkage studies in a Negro kindred with Norrie's disease.

W E Nance, S Hara, A Hansen, J Elliott, M Lewis, B Chown.   

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Year:  1969        PMID： 5307229      PMCID： PMC1706563     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN： 0002-9297            Impact factor:   11.025


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  14 in total

1.  Distribution of blood factors, ABO, MN and Rh in a group of American Negroes.

Authors:  R E MOORE
Journal:  Am J Phys Anthropol       Date:  1955-03       Impact factor: 2.868

2.  Norie's disease (atrofia bulborum hereditaria).

Authors:  M WARBURG
Journal:  Acta Ophthalmol (Copenh)       Date:  1963

3.  The Henshaw blood factor in New York City Negroes.

Authors:  W S POLLITZER
Journal:  Am J Phys Anthropol       Date:  1956-09       Impact factor: 2.868

4.  Sequential tests for the detection of linkage.

Authors:  N E MORTON
Journal:  Am J Hum Genet       Date:  1955-09       Impact factor: 11.025

5.  The incidence of multiple births in man and some of the other unipara.

Authors:  A F GUTTMACHER
Journal:  Obstet Gynecol       Date:  1953-07       Impact factor: 7.661

6.  Electrophoretic variation in human serum ceruloplasmin: a new genetic polymorphism.

Authors:  D C Shreffler; G J Brewer; J C Gall; M S Honeyman
Journal:  Biochem Genet       Date:  1967-09       Impact factor: 1.890

7.  Failure to detect linkage between Xg and other X-borne loci in Sardinians.

Authors:  M Siniscalco; G Filippi; B Latte; S Piomelli; M Rattazzi; J Gavin; R Sanger; R R Race
Journal:  Ann Hum Genet       Date:  1966-03       Impact factor: 1.670

8.  Norrie's disease.

Authors:  A C Hansen
Journal:  Am J Ophthalmol       Date:  1968-08       Impact factor: 5.258

9.  The linkage relation of Xg to g-6-pd in Israelis: the evidence of a second series of families.

Authors:  A Adam; P Tippett; J Gavin; J Noades; R Sanger; R R Race
Journal:  Ann Hum Genet       Date:  1967-01       Impact factor: 1.670

10.  Norrie's disease. A congenital progressive oculo-acoustico-cerebral degeneration.

Authors:  M Warburg
Journal:  Acta Ophthalmol (Copenh)       Date:  1966
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  7 in total

1.  Linkage analysis of Norrie disease with X-chromosomal ornithine aminotransferase.

Authors:  J B Bateman
Journal:  Trans Am Ophthalmol Soc       Date:  1992

2.  A presumptive new variant of Norrie's disease.

Authors:  C A Moreira-Filho; I Neustein
Journal:  J Med Genet       Date:  1979-04       Impact factor: 6.318

3.  Primary vitreoretinal dysplasia resembling Norrie's disease in a female: association with X autosome chromosomal translocation.

Authors:  N Ohba; T Yamashita
Journal:  Br J Ophthalmol       Date:  1986-01       Impact factor: 4.638

4.  Retinal dysplasia.

Authors:  V Godel; P Nemet; M Lazar
Journal:  Doc Ophthalmol       Date:  1981-07-15       Impact factor: 2.379

5.  Norrie disease gene is distinct from the monoamine oxidase genes.

Authors:  K B Sims; L Ozelius; T Corey; W B Rinehart; R Liberfarb; J Haines; W J Chen; R Norio; E Sankila; A de la Chapelle
Journal:  Am J Hum Genet       Date:  1989-09       Impact factor: 11.025

6.  Close linkage between Norrie disease, a cloned DNA sequence from the proximal short arm, and the centromere of the X chromosome.

Authors:  L M Bleeker-Wagemakers; U Friedrich; A Gal; T F Wienker; M Warburg; H H Ropers
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

Review 7.  A review of study designs and statistical methods for genomic epidemiology studies using next generation sequencing.

Authors:  Qian Wang; Qiongshi Lu; Hongyu Zhao
Journal:  Front Genet       Date:  2015-04-20       Impact factor: 4.599
  7 in total

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