(Q67285697)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6301974%20AND%20SRC:MED&resulttype=core&format=json

11 September 2019

title

Familial aniridia and translocation t(4;11)(q22;p13) without Wilms' tumor (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6301974%20AND%20SRC:MED&resulttype=core&format=json

11 September 2019

1 reference

K O Simola

1

1 reference

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11 September 2019

S Knuutila

2

1 reference

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11 September 2019

I Kaitila

3

1 reference

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11 September 2019

A Pirkola

4

1 reference

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11 September 2019

P Pohja

5

1 reference

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11 September 2019

publication date

1 January 1983

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11 September 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6301974%20AND%20SRC:MED&resulttype=core&format=json

11 September 2019

volume

63

1 reference

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11 September 2019

page(s)

158-161

1 reference

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11 September 2019

issue

2

1 reference

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https://scigraph.springernature.com/pub.10.1007/bf00291536

11 September 2019

exact match

0 references

cites work

Langer-Giedion syndrome with interstitial 8q-deletion

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

A deletion in chromosome 22 can cause DiGeorge syndrome

1 reference

12 December 2020

Familial retinoblastoma and chromosome 13 deletion transmitted via an insertional translocation.

1 reference

12 December 2020

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

1 reference

12 December 2020

Aniridia caused by a heritable chromosome 11 deletion.

1 reference

12 December 2020

Are balanced translocations really balanced? Preliminary cytogenetic evidence for position effect in man

1 reference

12 December 2020

[A new technic of analysis of the human karyotype]

1 reference

12 December 2020

Wilms' tumor in 75 year old male; report of a case

1 reference

12 December 2020

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

1 reference

12 December 2020

Partial triplication and deletion of 13q: study of a family presenting with bilateral retinoblastomas.

1 reference

12 December 2020

Chromosome 15 abnormalities and the Prader-Willi syndrome: a follow-up report of 40 cases

1 reference

12 December 2020

Autosomal dominant aniridia: probable linkage to acid phosphatase-1 locus on chromosome 2

1 reference

12 December 2020

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

1 reference

12 December 2020

ASSOCIATION OF WILMS'S TUMOR WITH ANIRIDIA, HEMIHYPERTROPHY AND OTHER CONGENITAL MALFORMATIONS

1 reference

12 December 2020

Catalase levels in patients with aniridia and/or Wilms' tumor: utility and limitations

1 reference

12 December 2020

1 reference

12 December 2020

Aniridia-Wilms tumor association

1 reference

12 December 2020

A rapid banding technique for human chromosomes

1 reference

12 December 2020

Association of del(11)(p15.1p12), aniridia, catalase deficiency, and cardiomyopathy.

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00291536

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6301974%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

11 September 2019

0 references

1 reference