Pericentric inversion (13) with two different recombinants in the same family. (Q33668164)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7205907%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

title

Pericentric inversion (13) with two different recombinants in the same family (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7205907%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

author name string

E M Williamson

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7205907%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

J F Miller

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7205907%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

M Seabright

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7205907%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

language of work or name

English

0 references

publication date

1 August 1980

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7205907%20AND%20SRC:MED&resulttype=core&format=json

Journal of Medical Genetics

13 October 2019

published in

1 reference

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13 October 2019

volume

17

1 reference

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13 October 2019

issue

4

1 reference

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13 October 2019

page(s)

309-312

1 reference

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Karyotype with chromosomal abnormality with various inherited defects in the offspring (Recombination aneusomy)

13 October 2019

cites work

1 reference

PubMed Central

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048576

Pericentric enversion of chromosome no. 13 in a large family leading to duplication deficiency causing congenital malformations in three individuals

21 June 2018

1 reference

PubMed Central

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048576

Familial pericentric inversion of chromosome 19, inv(19) (p13q13) with a note on genetic counseling of pericentric inversion carriers

21 June 2018

1 reference

PubMed Central

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048576

Patau's syndrome with D1 duplication‐deficiency derived from a maternal D group pericentric inversion

21 June 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/7205907

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Duplication/deficiency product of a pericentric inversion in man: A cause of D1 trisomy syndrome

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/7205907

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1136/JMG.17.4.309

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7205907%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7205907%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

PubMed publication ID

7205907

1 reference