(Q34211872)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7342404%20AND%20SRC:MED&resulttype=core&format=json

16 October 2019

title

Aniridia and mental retardation with deletion of the short arm of chromosome 11 (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7342404%20AND%20SRC:MED&resulttype=core&format=json

16 October 2019

1 reference

Kaiser-Kupfer MI

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7342404%20AND%20SRC:MED&resulttype=core&format=json

16 October 2019

White BJ

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7342404%20AND%20SRC:MED&resulttype=core&format=json

16 October 2019

Papadopoulos N

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7342404%20AND%20SRC:MED&resulttype=core&format=json

16 October 2019

publication date

1 January 1981

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7342404%20AND%20SRC:MED&resulttype=core&format=json

Transactions of the American Ophthalmological Society annual meeting

16 October 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7342404%20AND%20SRC:MED&resulttype=core&format=json

16 October 2019

volume

79

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7342404%20AND%20SRC:MED&resulttype=core&format=json

16 October 2019

page(s)

276-293

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7342404%20AND%20SRC:MED&resulttype=core&format=json

Ocular and Cerebral Abnormalities in Chromosome 18 Deletion Defect

16 October 2019

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1312188

Localization of the human lactate dehydrogenase B gene on the short arm of chromosome 12

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1312188

Assignment of three human genes to chromosomes (LDH-A to 11, TK to 17, and IDH to 20) and evidence for translocation between human and mouse chromosomes in somatic cell hybrids (thymidine kinase-lactate dehydrogenase A-isocitrate dehydrogenase-C-11,

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1312188

High Resolution of Human Chromosomes

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1312188

Assignments of the human genes for lactate dehydrogenase-A and thymidine kinase to specific chromosomal regions

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1312188

Dermatoglyphic and radiographic findings in a mother and daughter with pseudohypoparathyroidism

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1312188

Aniridia, cataract and gonadoblastoma in a mentally retarded girl with deletion of chromosome II. A clinicopathological case report

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1312188

Corneal Changes in Aniridia

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1312188

Aniridia Caused by a Heritable Chromosome 11 Deletion

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1312188

Aniridia-Wilms’ tumor association: evidence for specific deletion of 11p13

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1312188

The role of genetic factors in the etiology of wilms' tumor.Two pairs of monozygous twins with congenital abnormalities (Aniridia; hemihypertrophy) and discordance for wilms' tumor

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1312188

Aniridia, Cataracts, and wilms' Tumor in Monozygous Twins

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1312188

Chromosomal imbalance in the Aniridia-Wilms' tumor association: 11p interstitial deletion

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1312188

Ophthalmic Features of Chromosome Deletion 4p-(Wolf-Hirschhorn Syndrome)

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1312188

Ocular Abnormalities in the Cri Du Chat Syndrome

5 July 2018

1 reference

12 December 2020

Clinical applications of lactate dehydrogenase isoenzymes

1 reference

12 December 2020

Gene dose effect: intraband mapping of the <i>LDH A </i>locus using cells from four individuals with different interstitial deletions of 11p

1 reference

12 December 2020

Familial occurrence of the aniridia-Wilms tumor syndrome with deletion 11p13-14.1

1 reference

12 December 2020

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

1 reference

12 December 2020

Regional assignment of catalase (CAT) gene to band 11p13. Association with the aniridia-Wilms' tumor-Gonadoblastoma (WAGR) complex

1 reference

12 December 2020

Inkless methods of finger, palm, and sole printing

1 reference

12 December 2020

Hereditary deficiency of subunit H of lactate dehydrogenase

1 reference

12 December 2020

Identifiers

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7342404%20AND%20SRC:MED&resulttype=core&format=json

16 October 2019

PubMed publication ID

7342404

1 reference