Humoral immunodeficiency with facial dysmorphology and limb anomalies: a new syndrome-Reference-Cited by-同舟云学术

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Humoral immunodeficiency with facial dysmorphology and limb anomalies: a new syndrome

Published:2001-01 Issue:1 Volume:10 Page:1-8
ISSN:0962-8827
Container-title:Clinical Dysmorphology
language:en
Short-container-title:Clinical Dysmorphology

Author:

Hoffman Hal M.,Bastian John F.,Bird Lynne M.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Genetics (clinical),General Medicine,Pathology and Forensic Medicine,Anatomy,Pediatrics, Perinatology and Child Health

Reference22 articles.

1. Mulibrey nanism

2. Hallermann-Streiff syndrome: A review

3. Females with a disorder phenotypically identical to X-linked agammaglobulinemia

4. Predominance of sterile immunoglobulin transcripts in a female phenotypically resembling Bruton's agammaglobulinemia

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3. Disease-associated mutations in topoisomerase IIβ result in defective NK cells;Journal of Allergy and Clinical Immunology;2022-06

4. Update on Infections in Primary Antibody Deficiencies;Frontiers in Immunology;2021-02-11

5. Inherited TOP2B Mutation: Possible Confirmation of Mutational Hotspots in the TOPRIM Domain;Journal of Clinical Immunology;2021-01-18

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