(Q41937118)

14 October 2017

D13 ring chromosome syndrome (English)

1 reference

14 October 2017

Mccandless A

1

1 reference

14 October 2017

Walker S

series ordinal

2

1 reference

14 October 2017

language of work or name

English

0 references

publication date

1 June 1976

1 reference

Archives of Disease in Childhood

14 October 2017

1 reference

14 October 2017

51

1 reference

14 October 2017

6

1 reference

14 October 2017

449-453

1 reference

A ring D chromosome and anomalous inheritance of haptoglobin type

14 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1545995

D1 ring chromosome in newborn with peculiar face, polydactyly, imperforate anus, arrhinencephaly, and other malformations

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1545995

Symptomatology of the ring chromosomes of the D group. (2 new observations of type 13r)

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1545995

Comparative behavior of ring chromosomes

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1545995

The 13q-deletion syndrome

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1545995

The syndrome associated with the partial D-monosomy. Case report and review

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1545995

The 13q- deletion syndrome

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1545995

Ring 13 chromosome with normal haptoglobin inheritance

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1545995

Ring D 1 chromosome with remarkable morphological variation in a boy with mental retardation

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1545995

Malformative syndrome with ring chromosome 13.

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1545995

The behavior of ring chromosome 13.

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1545995

Syndrome associated with group-D chromosome deletions

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1545995

Ring chromosome 13 syndrome

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1545995

ABNORMALITIES WITH RING CHROMOSOME

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1545995

A rapid banding technique for human chromosomes

18 August 2018

1 reference

12 December 2020

Ring chromosome D (13) associated with multiple congenital malformations

1 reference

12 December 2020

A ring chromosome (46,XY,13r) occurring in a family with a D-D translocation 13-,14-, t(13q 14q)

1 reference

12 December 2020

Ring Chromosome D (13)

1 reference

12 December 2020

Identifiers

DOI

10.1136/ADC.51.6.449

1 reference

14 October 2017

1 reference

14 October 2017

PubMed publication ID

942238

1 reference