Localization of the Aland Island eye disease locus to the pericentromeric region of the X chromosome by linkage analysis.

scientific article

Localization of the Aland Island eye disease locus to the pericentromeric region of the X chromosome by linkage analysis. is …
instance of (P31):
scholarly articleQ13442814

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P932PMC publication ID1682761
P698PubMed publication ID1985461

P50authorAlbert de la ChapelleQ5618748
P2093author name stringEriksson AW
Alitalo T
Forsius H
Kruse TA
P2860cites workStrategies for multilocus linkage analysis in humansQ27860521
Easy calculations of lod scores and genetic risks on small computersQ29616143
A NEW EYE SYNDROME WITH X-CHROMOSOMAL TRANSMISSION. A FAMILY CLAN WITH FUNDUS ALBINISM, FOVEA HYPOPLASIA, NYSTAGMUS, MYOPIA, ASTIGMATISM AND DYSCHROMATOPSIAQ34258472
Assignment of the gene for complete X-linked congenital stationary night blindness (CSNB1) to Xp11.3.Q34465777
Report of the committee on linkage and gene orderQ34546618
Some notes on publications of Professor Arnold Sorsby and on Aland eye disease (Forsius-Eriksson syndrome)Q34633851
Analysis of human Y-chromosome-specific reiterated DNA in chromosome variantsQ35013854
An efficient strategy for gene mapping using multipoint linkage analysis: exclusion of the multiple endocrine neoplasia 2A (MEN2A) locus from chromosome 13.Q35198930
Isolation and characterization of a human variable copy number tandem repeat at Xcen-p11.22.Q35564631
Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms.Q35893411
Aland Island eye disease (Forsius-Eriksson syndrome) associated with contiguous deletion syndrome at Xp21. Similarity to incomplete congenital stationary night blindnessQ38671213
Report of the committee on the genetic constitution of the X chromosomeQ38695759
A model system for the analysis of gene exclusion: cystic fibrosis and chromosome 19.Q41887818
Congenital stationary night blindness with negative electroretinogram. A new classificationQ44444809
Aland Island eye disease (Forsius-Eriksson ocular albinism) and an Xp21 deletion in a patient with Duchenne muscular dystrophy, glycerol kinase deficiency, and congenital adrenal hypoplasia.Q52058110
A locus for X-linked congenital stationary night blindness is located on the proximal portion of the short arm of the X chromosomeQ60641499
Nystagmographical studies in Aland eye diseaseQ69130765
Gene of X-chromosomal congenital stationary night blindness is closely linked to DXS7 on XpQ69368565
Heterogeneity in the map distance between X-linked agammaglobulinemia and a map of nine RFLP lociQ69890191
X-linked retinoschisis is closely linked to DXS41 and DXS16 but not DXS85Q69904136
Forsius-Eriksson syndrome: its relation to the Nettleship-Falls X-linked ocular albinismQ71263506
Aland eye disease: no albino misroutingQ93658628
P433issue1
P407language of work or nameEnglishQ1860
P921main subjecteye diseaseQ3041498
P304page(s)31-38
P577publication date1991-01-01
P1433published inAmerican Journal of Human GeneticsQ4744249
P1476titleLocalization of the Aland Island eye disease locus to the pericentromeric region of the X chromosome by linkage analysis
P478volume48

Reverse relations

cites work (P2860)
Q37312045Aland island eye disease: clinical and electrophysiological studies of a Welsh family
Q24517919Conclusive evidence for a distinct congenital stationary night blindness locus in Xp21.1
Q24538863Evidence for genetic heterogeneity in X-linked congenital stationary night blindness.
Q37379790Genetic architecture of natural variation in visual senescence in Drosophila.
Q42659278Identification of a key recombinant which assigns the incomplete congenital stationary night blindness gene proximal to MAOB.
Q43168499Novel locus for X linked recessive high myopia maps to Xq23-q25 but outside MYP1.
Q35221170Refinement of the X-linked nonsyndromic high-grade myopia locus MYP1 on Xq28 and exclusion of 13 known positional candidate genes by direct sequencing
Q35196313Xp21 contiguous gene syndromes: deletion quantitation with bivariate flow karyotyping allows mapping of patient breakpoints

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