(Q35232185)

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The 13q-deletion syndrome

scientific article

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scholarly article

1 reference

Europe PubMed Central

7 August 2017

The 13q-deletion syndrome (English)

1 reference

Europe PubMed Central

7 August 2017

author name string

Allderdice PW

1

1 reference

Europe PubMed Central

7 August 2017

Davis JG

2

1 reference

Europe PubMed Central

7 August 2017

Miller OJ

3

1 reference

Europe PubMed Central

7 August 2017

Klinger HP

4

1 reference

Europe PubMed Central

7 August 2017

Warburton D

5

1 reference

Europe PubMed Central

7 August 2017

Miller DA

6

1 reference

Europe PubMed Central

7 August 2017

Allen FH Jr

7

1 reference

Europe PubMed Central

7 August 2017

Abrams CA

8

1 reference

Europe PubMed Central

7 August 2017

McGilvray E

9

1 reference

Europe PubMed Central

7 August 2017

language of work or name

0 references

publication date

1 September 1969

1 reference

Europe PubMed Central

7 August 2017

American Journal of Human Genetics

1 reference

Europe PubMed Central

7 August 2017

21

1 reference

Europe PubMed Central

7 August 2017

499-512

1 reference

Europe PubMed Central

7 August 2017

5

1 reference

Europe PubMed Central

7 August 2017

CHROMOSOME DELETION IN A CASE OF RETINOBLASTOMA.

1 reference

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

13 July 2018

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

1 reference

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

13 July 2018

A human ring D chromosome associated with multiple congenital abnormalities

1 reference

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

13 July 2018

A ring D chromosome and anomalous inheritance of haptoglobin type

1 reference

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

13 July 2018

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

1 reference

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

13 July 2018

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

1 reference

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

13 July 2018

ABNORMALITIES WITH RING CHROMOSOME

1 reference

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

26 September 2018

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/5347076

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/5347076

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/5347076

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/5347076

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multiple congenital abnormalities associated with ring chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/5347076

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ring Chromosomes in Human Beings

1 reference

https://pubmed.ncbi.nlm.nih.gov/5347076

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

PALM-PRINTS AND A RING-D CHROMOSOME

1 reference

https://pubmed.ncbi.nlm.nih.gov/5347076

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

1 reference

Europe PubMed Central

7 August 2017

1 reference

Europe PubMed Central

7 August 2017

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