(Q34164340)

English

Mapping the gene for X-linked cataracts and microcornea with facial, dental, and skeletal features to Xp22: an appraisal of the Nance-Horan syndrome.

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1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2576480%20AND%20SRC:MED&resulttype=core&format=json

1 October 2019

Mapping the gene for X-linked cataracts and microcornea with facial, dental, and skeletal features to Xp22: an appraisal of the Nance-Horan syndrome (English)

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2576480%20AND%20SRC:MED&resulttype=core&format=json

1 October 2019

1 reference

based on heuristic

inferred from title

author name string

Lewis RA

1

1 reference

Europe PubMed Central

PMC publication ID

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1 October 2019

publication date

1 January 1989

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2576480%20AND%20SRC:MED&resulttype=core&format=json

1 October 2019

Transactions of the American Ophthalmological Society annual meeting

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2576480%20AND%20SRC:MED&resulttype=core&format=json

1 October 2019

87

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2576480%20AND%20SRC:MED&resulttype=core&format=json

1 October 2019

658-728

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2576480%20AND%20SRC:MED&resulttype=core&format=json

1 October 2019

Organic-aciduria, decreased renal ammonia production, hydrophthalmos, and mental retardation; a clinical entity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298561

5 July 2018

The role of the sex chromosome in hereditary ocular pathology

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298561

5 July 2018

X-linked mental retardation: Renpenning revisited

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298561

5 July 2018

Human hypoxanthine-guanine phosphoribosyltransferase. Demonstration of structural variants in lymphoblastoid cells derived from patients with a deficiency of the enzyme

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298561

5 July 2018

Localization of loci for hypoxanthine phosphoribosyltransferase and glucose-6-phosphate dehydrogenase and biochemical evidence of nonrandom X chromosome expression from studies of a human X-autosome translocation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298561

5 July 2018

Genetics of microphthalmos

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298561

5 July 2018

Incontinentia pigmenti (Bloch-Sulzberger syndrome) and retinal changes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298561

5 July 2018

Strategies for multilocus linkage analysis in humans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298561

5 July 2018

The Nance-Horan syndrome: a rare X-linked ocular-dental trait with expression in heterozygous females

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298561

5 July 2018

A strategy to reveal high-frequency RFLPs along the human X chromosome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298561

5 July 2018

Close genetic linkage between X-linked retinitis pigmentosa and a restriction fragment length polymorphism identified by recombinant DNA probe L1.28

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298561

5 July 2018

DNA restriction fragment length polymorphisms and heterozygosity in the human genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298561

5 July 2018

Linkage analysis of two cloned DNA sequences flanking the Duchenne muscular dystrophy locus on the short arm of the human X chromosome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298561

5 July 2018

Probable assignment of the Duffy blood group locus to chromosome 1 in man

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298561

5 July 2018

X-linked colobomatous microphthalmos and other congenital anomalies. A disorder resembling Lenz's dysmorphogenetic syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298561

5 July 2018

Autosomal recessive oculocutaneous albinism in man. Evidence for genetic heterogeneity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298561

5 July 2018

Congenital X-linked cataract, dental anomalies and brachymetacarpalia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298561

5 July 2018

X-linked cataract: two pedigrees.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298561

5 July 2018

The biochemical basis for mucopolysaccharidoses and mucolipidoses

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298561

5 July 2018

Two cases of X/autosome translocation in females with incontinentia pigmenti.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298561

5 July 2018

The genetic linkage map of the human X chromosome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298561

5 July 2018

Rapid transfer of DNA from agarose gels to nylon membranes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298561

5 July 2018

Autosomal dominant cataract and microcornea associated with myopia in a Sicilian family

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298561

5 July 2018

A genetic linkage study of a kindred with X-linked retinitis pigmentosa

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298561

5 July 2018

A balanced de novo X/autosome translocation in a girl with manifestations of Lowe syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298561

5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298561

5 July 2018

Ocular findings in a new heritable syndrome of brain, eye, and urogenital abnormalities

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298561

5 July 2018

Multilocus linkage analysis in humans: detection of linkage and estimation of recombination

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298561

5 July 2018

Lenticular opacities in carriers of Lowe's syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298561

5 July 2018

Spontaneous mutation and parental age in humans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298561

5 July 2018

Fragile X syndrome: a unique mutation in man.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298561

5 July 2018

The 1987 Catalog of mapped genes and report of the nomenclature committee.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298561

5 July 2018

Linkage relationships between X-linked retinitis pigmentosa and nine short-arm markers: exclusion of the disease locus from Xp21 and localization to between DXS7 and DXS14.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298561

5 July 2018

Variable expressivity of autosomal dominant microcornea with cataract

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298561

5 July 2018

American paternal age data for selected years from 1876 to 1981.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298561

5 July 2018

Molecular cytogenetics: toward dissection of the contiguous gene syndromes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298561

5 July 2018

Efficient computations in multilocus linkage analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298561

5 July 2018

Incontinentia pigmenti (Bloch-Sulzberger syndrome): seven case reports from one family

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298561

5 July 2018

Contiguous gene syndromes: a component of recognizable syndromes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298561

5 July 2018

An RFLP detecting single copy X-chromosome fragment, dic56, from Xp22-Xpter [HGM8 assignment no. DXS 143].

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298561

5 July 2018

A study of restriction fragment length polymorphisms at the human alpha-1-antitrypsin locus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298561

5 July 2018

Normal human genomic restriction-fragment patterns and polymorphisms revealed by hybridization with the entire dystrophin cDNA.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298561

5 July 2018

Localization of the gene for X-linked recessive type of retinitis pigmentosa (XLRP) to Xp21 by linkage analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298561

5 July 2018

Tightly linked flanking markers for the Lowe oculocerebrorenal syndrome, with application to carrier assessment

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298561

5 July 2018

Multipoint linkage analysis of loci in the proximal long arm of the human X chromosome: application to mapping the choroideremia locus.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298561

5 July 2018

Mapping the Lowe oculocerebrorenal syndrome to Xq24-q26 by use of restriction fragment length polymorphisms

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298561

5 July 2018

Molecular detection of deletions involving band q14 of chromosome 13 in retinoblastomas

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298561

5 July 2018

Structural analysis of the X-linked gene encoding human glucose 6-phosphate dehydrogenase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298561

5 July 2018

The occurrence of new mutants in the X-linked recessive Lesch-Nyhan disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298561

5 July 2018

Detection of specific sequences among DNA fragments separated by gel electrophoresis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298561

5 July 2018

Lowe's syndrome: identification of carriers by lens examination

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298561

5 July 2018

A Family with X-Chromosomal Recessive Congenital Cataract, Microphthalmia, a Peculiar Form of the Ear and Dental Anomalies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298561

5 July 2018

Evidence for a Null allele at the Esterase D (EC 3.1.1.1) locus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298561

5 July 2018

Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298561

5 July 2018

Classification of Hereditary Cataracts in Children by Linkage Analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298561

5 July 2018

The Ocular Manifestations in Fabry's Disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298561

5 July 2018

Apert's syndrome (a type of acrocephalosyndactyly)-observations on a British series of thirty-nine cases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298561

28 October 2018

[Recessive, sex-limited microphthalmia with multiple abnormalities]

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298561

28 October 2018

Close linkage of fragile X-mental retardation syndrome to haemophilia B and transmission through a normal male

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298561

28 October 2018

The pathophysiology of neurofibromatosis: IX. Paternal age as a factor in the origin of new mutations.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298561

28 October 2018

Norrie's disease: a study of two families.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298561

28 October 2018

Two anonymous DNA segments distinguish the Wilms' tumor and aniridia loci

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1298561

28 October 2018

Genetic linkage study between the loci for Duchenne and Becker muscular dystrophy and nine X-chromosomal DNA markers

1 reference

https://pubmed.ncbi.nlm.nih.gov/2576480

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital cataract with microcornea and Peters' anomaly as expressions of one autosomal dominant gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/2576480

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Parental age effects on the occurrence of new mutations for the Marfan syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/2576480

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Spontaneous mutation in man

1 reference

https://pubmed.ncbi.nlm.nih.gov/2576480

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autosomal dominant cataracts and microcornea

1 reference

https://pubmed.ncbi.nlm.nih.gov/2576480

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cataracts as a marker of genetic heterogeneity in chondrodysplasia punctata

1 reference

https://pubmed.ncbi.nlm.nih.gov/2576480

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ocular manifestations in a family with probably X-linked cataracts

1 reference

https://pubmed.ncbi.nlm.nih.gov/2576480

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Is there an X-linked form of congenital cataracts?

1 reference

https://pubmed.ncbi.nlm.nih.gov/2576480

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The contribution of chromosome aberrations to the precision of human gene mapping

1 reference

https://pubmed.ncbi.nlm.nih.gov/2576480

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Agenesis of corpus callosum, ocular, and skeletal anomalies (X-linked dominant Aicardi's syndrome) in a girl with balanced X/3 translocation

1 reference

https://pubmed.ncbi.nlm.nih.gov/2576480

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sectorial cataract: a possible example of lyonisation

1 reference

https://pubmed.ncbi.nlm.nih.gov/2576480

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A primary genetic map of markers of human chromosome 10

1 reference

https://pubmed.ncbi.nlm.nih.gov/2576480

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Heteromorphic X chromosomes in 46,XX males: Evidence for the involvement of X-Y interchange

1 reference

https://pubmed.ncbi.nlm.nih.gov/2576480

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Regional assignment of genes for human esterase D and retinoblastoma to chromosome band 13q14

1 reference

https://pubmed.ncbi.nlm.nih.gov/2576480

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analysis of linkage relationships of X-linked retinitis pigmentosa with the following Xp loci: L1.28, OTC, 754, XJ-1.1, pERT87, and C7

1 reference

https://pubmed.ncbi.nlm.nih.gov/2576480

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-linked retinitis pigmentosa. Profile of clinical findings

1 reference

https://pubmed.ncbi.nlm.nih.gov/2576480

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Report of the committee on the genetic constitution of the X and Y chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/2576480

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Report of the committee on human gene mapping by recombinant DNA techniques

1 reference

https://pubmed.ncbi.nlm.nih.gov/2576480

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary microcornea and cataract in five generations

1 reference

https://pubmed.ncbi.nlm.nih.gov/2576480

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Heredofamilial bilateral anophthalmia

1 reference

https://pubmed.ncbi.nlm.nih.gov/2576480

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

PROBABLE LINKAGE BETWEEN A CONGENITAL CATARACT LOCUS AND THE DUFFY BLOOD GROUP LOCUS

1 reference

https://pubmed.ncbi.nlm.nih.gov/2576480

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

HEREDITARY CATARACTS AND MICROPHTHALMIA

1 reference

https://pubmed.ncbi.nlm.nih.gov/2576480

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Growth of the components of the human eyeball; II. Comparison of the calculated volumes of the eyes of the newborn and of adults, and their components

1 reference

https://pubmed.ncbi.nlm.nih.gov/2576480

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lowe's syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/2576480

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-Linked cataract

1 reference

https://pubmed.ncbi.nlm.nih.gov/2576480

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The effect of the age of the father at conception on the mutations to hemphilia A

1 reference

https://pubmed.ncbi.nlm.nih.gov/2576480

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-Chromosomal-Linked Sutural Cataracts

1 reference

https://pubmed.ncbi.nlm.nih.gov/2576480

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-linked dominant chondrodysplasia punctata: a case report and family studies

1 reference

https://pubmed.ncbi.nlm.nih.gov/2576480

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mapping X-linked ophthalmic diseases: II. Linkage relationship of X-linked retinitis pigmentosa to X chromosomal short arm markers

1 reference

https://pubmed.ncbi.nlm.nih.gov/2576480

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mapping X-linked ophthalmic diseases. Provisional assignment of the locus for choroideremia to Xq13-q24

1 reference

https://pubmed.ncbi.nlm.nih.gov/2576480

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Report of the Committee on Methods of Linkage Analysis and Reporting

1 reference

https://pubmed.ncbi.nlm.nih.gov/2576480

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cytogenetic heterogeneity of translocations associated with Duchenne muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/2576480

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Choroideremia-locus maps between DXS3 and DXS11 on Xq

1 reference

https://pubmed.ncbi.nlm.nih.gov/2576480

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2576480%20AND%20SRC:MED&resulttype=core&format=json

1 October 2019

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2576480%20AND%20SRC:MED&resulttype=core&format=json

1 October 2019

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