Literature DB >> 3857130

Norrie's disease: close linkage with genetic markers from the proximal short arm of the X chromosome.

A Gal, C Stolzenberger, T Wienker, P Wieacker, H H Ropers, U Friedrich, L Bleeker-Wagemakers, P Pearson, M Warburg.   

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Year:  1985        PMID： 3857130     DOI： 10.1111/j.1399-0004.1985.tb00221.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN： 0009-9163            Impact factor:   4.438


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  15 in total

1.  The ocular pathology of Norrie disease in a fetus of 11 weeks' gestational age.

Authors:  M A Parsons; D Curtis; C E Blank; H N Hughes; A C McCartney
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  1992       Impact factor: 3.117

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

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

3.  Genes for synapsin I, a neuronal phosphoprotein, map to conserved regions of human and murine X chromosomes.

Authors:  T L Yang-Feng; L J DeGennaro; U Francke
Journal:  Proc Natl Acad Sci U S A       Date:  1986-11       Impact factor: 11.205

Review 4.  X linked mental retardation.

Authors:  I A Glass
Journal:  J Med Genet       Date:  1991-06       Impact factor: 6.318

5.  Defining DNA diagnostic tests appropriate or standard clinical care.

Authors:  R V Lebo; G Cunningham; M J Simons; L J Shapiro
Journal:  Am J Hum Genet       Date:  1990-09       Impact factor: 11.025

Review 6.  Molecular genetics of the human X chromosome.

Authors:  K E Davies
Journal:  J Med Genet       Date:  1985-08       Impact factor: 6.318

7.  Linkage analysis of Norrie disease with an X-chromosomal ornithine aminotransferase locus.

Authors:  J B Bateman; T L Kojis; R M Cantor; C Heinzmann; J T Ngo; M A Spence; G Inana; J D Kivlin; D Curtis; R S Sparkes
Journal:  Trans Am Ophthalmol Soc       Date:  1993

8.  Norrie disease resulting from a gene deletion: clinical features and DNA studies.

Authors:  D Donnai; R C Mountford; A P Read
Journal:  J Med Genet       Date:  1988-02       Impact factor: 6.318

Review 9.  Molecular genetics of retinitis pigmentosa.

Authors:  D B Farber; J R Heckenlively; R S Sparkes; J B Bateman
Journal:  West J Med       Date:  1991-10

10.  Clinical reinvestigation and linkage analysis in the family with Episkopi blindness (Norrie disease).

Authors:  G Wolff; A Mayerová; T F Wienker; P Atalianis; P Ioannou; M Warburg
Journal:  J Med Genet       Date:  1992-11       Impact factor: 6.318
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