(Q53153093)

English

Diagnosis of 22q11.2 deletion syndrome and artemis deficiency in two children with T-B-NK+ immunodeficiency.

scientific article published on 3 August 2012

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

11 May 2018

http://europepmc.org/abstract/MED/22864628

Diagnosis of 22q11.2 deletion syndrome and artemis deficiency in two children with T-B-NK+ immunodeficiency. (English)

1 reference

Europe PubMed Central

PubMed publication ID

11 May 2018

http://europepmc.org/abstract/MED/22864628

artemis deficiency

1 reference

based on heuristic

inferred from title

Jean-Pierre de Villartay

7

1 reference

Europe PubMed Central

PubMed publication ID

11 May 2018

http://europepmc.org/abstract/MED/22864628

Despina Moshous

8

1 reference

Europe PubMed Central

PubMed publication ID

11 May 2018

http://europepmc.org/abstract/MED/22864628

Donna M McDonald-McGinn

5

object named as

Donna McDonald-McGinn

1 reference

Europe PubMed Central

PubMed publication ID

11 May 2018

http://europepmc.org/abstract/MED/22864628

author name string

Jennifer Heimall

1

1 reference

Europe PubMed Central

PubMed publication ID

11 May 2018

http://europepmc.org/abstract/MED/22864628

Michael Keller

2

1 reference

Europe PubMed Central

PubMed publication ID

11 May 2018

http://europepmc.org/abstract/MED/22864628

Rushani Saltzman

3

1 reference

Europe PubMed Central

PubMed publication ID

11 May 2018

http://europepmc.org/abstract/MED/22864628

Nancy Bunin

4

1 reference

Europe PubMed Central

PubMed publication ID

11 May 2018

http://europepmc.org/abstract/MED/22864628

Elaine Zakai

6

1 reference

Europe PubMed Central

PubMed publication ID

11 May 2018

http://europepmc.org/abstract/MED/22864628

Barbara Ariue

9

1 reference

Europe PubMed Central

PubMed publication ID

11 May 2018

http://europepmc.org/abstract/MED/22864628

Elizabeth A McCarthy

10

1 reference

Europe PubMed Central

PubMed publication ID

11 May 2018

http://europepmc.org/abstract/MED/22864628

Blythe H Devlin

11

1 reference

Europe PubMed Central

PubMed publication ID

11 May 2018

http://europepmc.org/abstract/MED/22864628

Suhag Parikh

12

1 reference

Europe PubMed Central

PubMed publication ID

11 May 2018

http://europepmc.org/abstract/MED/22864628

Rebecca H Buckley

13

1 reference

Europe PubMed Central

PubMed publication ID

11 May 2018

http://europepmc.org/abstract/MED/22864628

M Louise Markert

14

1 reference

Europe PubMed Central

PubMed publication ID

11 May 2018

http://europepmc.org/abstract/MED/22864628

publication date

3 August 2012

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Europe PubMed Central

PubMed publication ID

11 May 2018

http://europepmc.org/abstract/MED/22864628

Journal of Clinical Immunology

1 reference

Europe PubMed Central

PubMed publication ID

11 May 2018

http://europepmc.org/abstract/MED/22864628

32

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Europe PubMed Central

PubMed publication ID

11 May 2018

http://europepmc.org/abstract/MED/22864628

5

1 reference

Europe PubMed Central

PubMed publication ID

11 May 2018

http://europepmc.org/abstract/MED/22864628

1141-1144

1 reference

Europe PubMed Central

PubMed publication ID

11 May 2018

http://europepmc.org/abstract/MED/22864628

https://scigraph.springernature.com/pub.10.1007/s10875-012-9741-9

0 references

Transplantation of hematopoietic stem cells in human severe combined immunodeficiency: longterm outcomes

1 reference

https://api.crossref.org/works/10.1007%2FS10875-012-9741-9

21 January 2018

Review of 54 patients with complete DiGeorge anomaly enrolled in protocols for thymus transplantation: outcome of 44 consecutive transplants

1 reference

https://api.crossref.org/works/10.1007%2FS10875-012-9741-9

21 January 2018

DiGeorge anomaly in the absence of chromosome 22q11.2 deletion

1 reference

https://api.crossref.org/works/10.1007%2FS10875-012-9741-9

21 January 2018

Chromosome 22q11.2 deletion syndrome: DiGeorge syndrome/velocardiofacial Syndrome.

1 reference

https://api.crossref.org/works/10.1007%2FS10875-012-9741-9

21 January 2018

A founder mutation in Artemis, an SNM1-like protein, causes SCID in Athabascan-speaking Native Americans

1 reference

https://api.crossref.org/works/10.1007%2FS10875-012-9741-9

21 January 2018

Hematopoietic stem cell transplantation for severe combined immunodeficiency in the neonatal period leads to superior thymic output and improved survival

1 reference

https://pubmed.ncbi.nlm.nih.gov/22864628

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S10875-012-9741-9

1 reference

Europe PubMed Central

PubMed publication ID

11 May 2018

http://europepmc.org/abstract/MED/22864628

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

11 May 2018

http://europepmc.org/abstract/MED/22864628

ResearchGate publication ID

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