(Q33681032)

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Mosaicism for a tandem duplication dup(1)(q12q22) in an 18 year old female

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

1 reference

Europe PubMed Central

Mosaicism for a tandem duplication dup(1)(q12q22) in an 18 year old female (English)

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

author name string

de Silva D

1

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Massie D

2

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Drummond J

3

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Couzin D

4

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Dean JC

5

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Europe PubMed Central

PubMed publication ID

28 July 2017

language of work or name

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publication date

1 July 1998

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Europe PubMed Central

PubMed publication ID

28 July 2017

Journal of Medical Genetics

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Europe PubMed Central

PubMed publication ID

28 July 2017

35

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

7

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

600-603

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Proteus syndrome: clinical evidence for somatic mosaicism and selective review

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051373

21 June 2018

Cytogenetic and molecular analysis of a de novo tandem duplication of chromosome 21

1 reference

https://pubmed.ncbi.nlm.nih.gov/9678707

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Selective deficiency of antibody responses to polysaccharide antigens in a child mosaic for partial trisomy 1 (46,XX,dir dup (1) (q12----q23)/46,XX)

1 reference

https://pubmed.ncbi.nlm.nih.gov/9678707

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Tandem duplication (1) (q11----q22) in a male infant with multiple congenital malformations

1 reference

https://pubmed.ncbi.nlm.nih.gov/9678707

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Report of a case resembling the Proteus syndrome with a chromosome abnormality

1 reference

https://pubmed.ncbi.nlm.nih.gov/9678707

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cutaneous manifestation of lethal genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/9678707

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1136/JMG.35.7.600

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

ResearchGate publication ID

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