(Q41634920)

English

X-linked ocular albinism: a family containing a manifesting heterozygote, and an affected male married to a female with autosomal recessive ocular albinism

scientific article published on January 1981

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

5 October 2017

X-linked ocular albinism: a family containing a manifesting heterozygote, and an affected male married to a female with autosomal recessive ocular albinism (English)

1 reference

Europe PubMed Central

PubMed publication ID

5 October 2017

1 reference

based on heuristic

inferred from title

ocular albinism

1 reference

based on heuristic

inferred from title

author name string

C Jaeger

1

1 reference

Europe PubMed Central

PubMed publication ID

5 October 2017

B Jay

2

1 reference

Europe PubMed Central

PubMed publication ID

5 October 2017

publication date

1 January 1981

1 reference

Europe PubMed Central

PubMed publication ID

5 October 2017

1 reference

Europe PubMed Central

PubMed publication ID

5 October 2017

56

1 reference

Europe PubMed Central

PubMed publication ID

5 October 2017

3

1 reference

Europe PubMed Central

PubMed publication ID

5 October 2017

299-304

1 reference

Europe PubMed Central

PubMed publication ID

5 October 2017

https://scigraph.springernature.com/pub.10.1007/bf00274683

0 references

Autosomal recessively inherited ocular albinism. A new form of ocular albinism affecting females as severely as males

1 reference

https://pubmed.ncbi.nlm.nih.gov/7239514

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-chromosomal ocular albinism in a Dutch family

1 reference

https://pubmed.ncbi.nlm.nih.gov/7239514

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Macromelanosomes in X-linked ocular albinism

1 reference

https://pubmed.ncbi.nlm.nih.gov/7239514

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-linked ocular albinism. An oculocutaneous macromelanosomal disorder.

1 reference

https://pubmed.ncbi.nlm.nih.gov/7239514

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A NEW EYE SYNDROME WITH X-CHROMOSOMAL TRANSMISSION. A FAMILY CLAN WITH FUNDUS ALBINISM, FOVEA HYPOPLASIA, NYSTAGMUS, MYOPIA, ASTIGMATISM AND DYSCHROMATOPSIA

1 reference

https://pubmed.ncbi.nlm.nih.gov/7239514

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

1 reference

https://pubmed.ncbi.nlm.nih.gov/7239514

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-linked ocular albinism in Blacks. Ocular albinism cum pigmento

1 reference

https://pubmed.ncbi.nlm.nih.gov/7239514

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

CARRIERS OF OCULAR ALBINISM WITH AND WITHOUT OCULAR CHANGES

1 reference

https://pubmed.ncbi.nlm.nih.gov/7239514

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gene action in the X-chromosome of the mouse (Mus musculus L.)

1 reference

https://pubmed.ncbi.nlm.nih.gov/7239514

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sex-linked ocular albinism displaying typical fundus changes in the female heterozygote

1 reference

https://pubmed.ncbi.nlm.nih.gov/7239514

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00274683

1 reference

Europe PubMed Central

PubMed publication ID

5 October 2017

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

5 October 2017

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q41634920&oldid=1925359074"