A homozygote for pericentric inversion of chromosome 4. (Q33670074)

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28 October 2019

title

A homozygote for pericentric inversion of chromosome 4 (English)

1 reference

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28 October 2019

author name string

N J Carpenter

series ordinal

1

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28 October 2019

B Say

series ordinal

2

1 reference

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28 October 2019

N D Barber

series ordinal

3

1 reference

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28 October 2019

language of work or name

English

0 references

publication date

1 December 1982

1 reference

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Journal of Medical Genetics

28 October 2019

published in

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28 October 2019

volume

19

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28 October 2019

issue

6

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28 October 2019

page(s)

469-471

1 reference

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Deletions of different segments of the long arm of chromosome 4.

28 October 2019

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048967

Inherited pericentric inversion of chromosome no. 4.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048967

Heterozygosity and homozygosity for a pericentric inversion of human chromosone 3

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048967

Trisomy 4p due to recombination aneusomy of an inversion 4 (p 14, q 35)

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048967

Pericentric inversions of human chromosomes 9 and 10.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048967

Dominant piebald trait in a retarded child with a reciprocal translocation and small intercalary deletion.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048967

Structural variation in chromosome No 9.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048967

Chromosome 3 duplication q21 leads to qter deletion p25 leads to pter syndrome in children of carriers of a pericentric inversion inv(3) (p25q21)

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048967

Cytological assessment of meiotic exchange in a human male with a pericentric inversion of chromosome No. 4

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048967

Partial monosomy and partial trisomy 18 in two offspring of carrier of pericentric inversion of chromosome 18

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048967

The Wolf-Hirschhorn (4p-) syndrome.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048967

Inversion homozygosity of chromosome no. 9 in a higly inbred kindred

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048967

Pericentric inversions of chromosome 9 in two families

21 June 2018

1 reference

12 December 2020

Inherited pericentric inversion of chromosome 5: a family with history of neonatal death and a case of the "cri du chat" syndrome

1 reference

12 December 2020

Pericentric inversion of chromosome 4 : inv (4) (p13, q35) and trisomy of the short branch of chromosome 4 due to recombination aneusomy

1 reference

12 December 2020

A pericentric inversion of a chromosome 4 with a t(4q 10p-) and a familial t(DqDq) in a mentally retarded girl

1 reference

12 December 2020

Human Q and C chromosomal variations: distribution and incidence

1 reference

12 December 2020

Association of pericentric inversion of chromosome 9 and reproductive failure in ten unrelated families

1 reference

12 December 2020

Proximal 4p-deletion: phenotype differs from classical 4p-syndrome

1 reference

12 December 2020

Pericentric inversion and partial monosomy 4q associated with congenital anomalies

1 reference

12 December 2020

Identifiers

DOI

10.1136/JMG.19.6.469

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6185681 AND SRC:MED&resulttype=core&format=json

28 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6185681 AND SRC:MED&resulttype=core&format=json

28 October 2019

PubMed publication ID

6185681

1 reference