(Q33592792)

28 July 2017

Interstitial deletion of distal 13q associated with Hirschsprung's disease (English)

1 reference

28 July 2017

Hirschsprung's disease

1 reference

Lamont MA

1

1 reference

28 July 2017

Fitchett M

series ordinal

2

1 reference

28 July 2017

Dennis NR

series ordinal

3

1 reference

28 July 2017

language of work or name

English

0 references

publication date

1 February 1989

1 reference

Journal of Medical Genetics

28 July 2017

1 reference

28 July 2017

26

1 reference

28 July 2017

100-104

1 reference

28 July 2017

2

1 reference

Retinoblastoma and Subband Deletion of Chromosome 13

28 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015558

13q- syndrome. Family study

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015558

Interstitial deletion 13q syndromes: a report on two unrelated patients.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015558

Hirschsprung's disease and Waardenburg's syndrome

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015558

Interstitial deletion of long arm of chromosome 13.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015558

A rapid banding technique for human chromosomes

30 October 2018

1 reference

12 December 2020

Retinoblastoma, gross internal malformations, and deletion 13q14 leads to q31

1 reference

12 December 2020

The ring chromosome 13 syndrome

1 reference

12 December 2020

A 13q- syndrome with extensive intestinal atresia

1 reference

12 December 2020

Identifiers

PMCID

1015558

1 reference

28 July 2017

1 reference