Prenatal diagnosis and follow up of a child with a complex chromosome rearrangement (Q33672683)

28 July 2017

title

Prenatal diagnosis and follow up of a child with a complex chromosome rearrangement (English)

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28 July 2017

Bogart MH

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28 July 2017

Bradshaw CL

series ordinal

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28 July 2017

Jones OW

series ordinal

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28 July 2017

Schanberger JE

series ordinal

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28 July 2017

language of work or name

English

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publication date

1 April 1986

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Journal of Medical Genetics

28 July 2017

published in

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28 July 2017

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28 July 2017

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28 July 2017

page(s)

180-183

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A complex rearrangement involving three autosomes in a phenotypically normal male presenting with sterility.

28 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049579

A complex double translocation involving four chromosomes and five breakpoints in a child with mild mental retardation.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049579

A case of multiple chromosomal rearrangements with persistence of foetal haemoglobin

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049579

A familial reciprocal translocation between three chromosomes.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049579

Complex translocation t(9;21)(9;22)(q12p13)(q12q11) in the family of a child with 9p trisomy 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=1049579

A complex translocation involving chromosomes 3,11, and 14 with an interstitial deletion, del(14) (q13q22) in a child with congenital glaucoma and cleft lip and palate

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049579

Familial balanced (7;11;21)translocation and Down's syndrome in two siblings

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049579

De novo translocation heterozygote with three reciprocal translocations

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049579

Familial translocation involving chromosome 6, 14 and 20, identified by quinacrine fluorescence

30 October 2018

1 reference

12 December 2020

Partial trisomy 11 in a child resulting from a complex maternal rearrangement of chromosomes 11, 12 and 13

1 reference

12 December 2020

Possible complex translocation t(9;14;13) (q12;pl?;Q31) in mother of a child with 9-p trisomy syndrome

1 reference

12 December 2020

Partial trisomy 11,46,XX,-3,-20,+der3,+der20,t(3:11:20), resulting from a complex maternal rearrangement of chromosomes 3, 11, 20

1 reference

12 December 2020

Trisomy 9p due to a maternal complex translocation involving chromosomes 4, 6 and 9

1 reference

12 December 2020

Rearrangements involving four chromosomes in a child with congenital abnormalities

1 reference

12 December 2020

Partial trisomy of chromosome 1 resulting from a complex maternal rearrangement of chromosomes 1, 5, and 6

1 reference

12 December 2020

[Maternal translocation t (1; 8; 15) and trisomy 8 qter in her daughter. Genetic counseling]

1 reference

12 December 2020

Complex balanced translocation of chromosomes 2,3, and 13

1 reference

12 December 2020

A complex familial translocation involving chromosomes 5, 9 and 13

1 reference

12 December 2020

Identifiers

PMC publication ID

1049579

1 reference

28 July 2017

1 reference