MRI findings in a patient with partial monosomy 10p. (Q33680246)

28 July 2017

title

MRI findings in a patient with partial monosomy 10p. (English)

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28 July 2017

Sunada F

1

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28 July 2017

Rash FC

series ordinal

2

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28 July 2017

Tam DA

series ordinal

3

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28 July 2017

language of work or name

English

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publication date

1 February 1998

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Journal of Medical Genetics

28 July 2017

published in

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28 July 2017

volume

35

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28 July 2017

issue

2

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28 July 2017

page(s)

159-161

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A clinical and molecular study of mosaicism for trisomy 17.

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=1051224

DiGeorge syndrome and partial monosomy 10p: case report and review

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051224

Family with partial monosomy 10p and trisomy 10p.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051224

[Partial monosomy 10p in a case investigated with tomodensitometry (author's transl)]

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051224

Partial monosomy of chromosome 10 short arms.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051224

Further delineation of the 10p deletion 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=1051224

Partial deletion 10p syndrome. Report of two patients.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051224

Molecular cytogenetic analysis of a familial 8p23.1 deletion associated with minimal dysmorphic features, seizures, and 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=1051224

Del(10)p autosomal deletion syndrome: Clinical, cytogenetic and gene marker studies

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051224

Deletion of the short arm of chromosome No. 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=1051224

Partial monosomy 10p 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=1051224

A common region of 10p deleted in DiGeorge and velocardiofacial syndromes

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051224

C-group chromosome abnormality (? 10p-). Occurrence in a child with multiple malformations

30 October 2018

1 reference

12 December 2020

Deletion of the short arm of chromosome No. 10

1 reference

12 December 2020

Hypoparathyroidism and T cell immune defect in a patient with 10p deletion syndrome

1 reference

12 December 2020

1 reference

12 December 2020

A case of de novo translocation 7; 10 and the duplication 7p, deletion 10p phenotype

1 reference

12 December 2020

4p- Syndrome: A Chromosomal Disorder Associated with a Particular EEG Pattern

1 reference

12 December 2020

Identifiers

DOI

10.1136/JMG.35.2.159

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28 July 2017

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28 July 2017

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