scholarly article | Q13442814 |
P50 | author | Albert de la Chapelle | Q5618748 |
P2093 | author name string | Eriksson AW | |
Alitalo T | |||
Forsius H | |||
Kruse TA | |||
P2860 | cites work | Strategies for multilocus linkage analysis in humans | Q27860521 |
Easy calculations of lod scores and genetic risks on small computers | Q29616143 | ||
A NEW EYE SYNDROME WITH X-CHROMOSOMAL TRANSMISSION. A FAMILY CLAN WITH FUNDUS ALBINISM, FOVEA HYPOPLASIA, NYSTAGMUS, MYOPIA, ASTIGMATISM AND DYSCHROMATOPSIA | Q34258472 | ||
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 order | Q34546618 | ||
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 variants | Q35013854 | ||
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 blindness | Q38671213 | ||
Report of the committee on the genetic constitution of the X chromosome | Q38695759 | ||
A model system for the analysis of gene exclusion: cystic fibrosis and chromosome 19. | Q41887818 | ||
Congenital stationary night blindness with negative electroretinogram. A new classification | Q44444809 | ||
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 chromosome | Q60641499 | ||
Nystagmographical studies in Aland eye disease | Q69130765 | ||
Gene of X-chromosomal congenital stationary night blindness is closely linked to DXS7 on Xp | Q69368565 | ||
Heterogeneity in the map distance between X-linked agammaglobulinemia and a map of nine RFLP loci | Q69890191 | ||
X-linked retinoschisis is closely linked to DXS41 and DXS16 but not DXS85 | Q69904136 | ||
Forsius-Eriksson syndrome: its relation to the Nettleship-Falls X-linked ocular albinism | Q71263506 | ||
Aland eye disease: no albino misrouting | Q93658628 | ||
P433 | issue | 1 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | eye disease | Q3041498 |
P304 | page(s) | 31-38 | |
P577 | publication date | 1991-01-01 | |
P1433 | published in | American Journal of Human Genetics | Q4744249 |
P1476 | title | Localization of the Aland Island eye disease locus to the pericentromeric region of the X chromosome by linkage analysis | |
P478 | volume | 48 |
Q37312045 | Aland island eye disease: clinical and electrophysiological studies of a Welsh family |
Q24517919 | Conclusive evidence for a distinct congenital stationary night blindness locus in Xp21.1 |
Q24538863 | Evidence for genetic heterogeneity in X-linked congenital stationary night blindness. |
Q37379790 | Genetic architecture of natural variation in visual senescence in Drosophila. |
Q42659278 | Identification of a key recombinant which assigns the incomplete congenital stationary night blindness gene proximal to MAOB. |
Q43168499 | Novel locus for X linked recessive high myopia maps to Xq23-q25 but outside MYP1. |
Q35221170 | Refinement of the X-linked nonsyndromic high-grade myopia locus MYP1 on Xq28 and exclusion of 13 known positional candidate genes by direct sequencing |
Q35196313 | Xp21 contiguous gene syndromes: deletion quantitation with bivariate flow karyotyping allows mapping of patient breakpoints |
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