(Q35232185)

7 August 2017

title

The 13q-deletion syndrome (English)

1 reference

7 August 2017

Allderdice PW

1

1 reference

7 August 2017

Davis JG

2

1 reference

7 August 2017

Miller OJ

3

1 reference

7 August 2017

Klinger HP

4

1 reference

7 August 2017

Warburton D

5

1 reference

7 August 2017

Miller DA

6

1 reference

7 August 2017

Allen FH Jr

7

1 reference

7 August 2017

Abrams CA

8

1 reference

7 August 2017

McGilvray E

9

1 reference

7 August 2017

language of work or name

English

0 references

publication date

1 September 1969

1 reference

American Journal of Human Genetics

7 August 2017

published in

1 reference

7 August 2017

volume

21

1 reference

7 August 2017

issue

5

1 reference

7 August 2017

page(s)

499-512

1 reference

CHROMOSOME DELETION IN A CASE OF RETINOBLASTOMA.

7 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706574

Absent thumbs with a ring D2 chromosome: a new deletion syndrome

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706574

A human ring D chromosome associated with multiple congenital abnormalities

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706574

A ring D chromosome and anomalous inheritance of haptoglobin type

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706574

Autosomal trisomy syndromes: a detailed study of 27 cases of Edwards' syndrome and 27 cases of Patau's syndrome

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706574

The Dr phenotype: a study of threee cases with a ring D chromosome

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706574

ABNORMALITIES WITH RING CHROMOSOME

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706574

The upper limb-cardiovascular syndrome. An autosomal dominant genetic effect on embryogenesis

26 September 2018

1 reference

12 December 2020

The identification of the chromosomes of the D group (13-15) Denver: an autoradiographic and measurement study

1 reference

12 December 2020

Partial deletion of the long arm of a group D (13-15) chromosome :Dq-

1 reference

12 December 2020

Ring D chromosome: a second case associated with anomalous haptoglobin inheritance

1 reference

12 December 2020

Multiple congenital abnormalities associated with ring chromosome

1 reference

12 December 2020

Ring Chromosomes in Human Beings

1 reference

12 December 2020

PALM-PRINTS AND A RING-D CHROMOSOME

1 reference

12 December 2020

Identifiers

PMC publication ID

1706574

1 reference

7 August 2017

1 reference