Open AccessClinical characteristics and immunological status of patients with 22q11.2 deletion syndrome in Northern Thailand
Author(s) -
Thanida Uaareechit,
Pairada Varnado,
Maliwan Tengsujaritkul,
Orawan Louthrenoo,
Yupada Pongprot,
Mongkol LaoAraya
Publication year - 2020
Publication title -
asian pacific journal of allergy and immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.405
H-Index - 33
ISSN - 0125-877X
DOI - 10.12932/ap-241019-0671
Subject(s) - tetralogy of fallot , medicine , genitourinary system , pediatrics , intellectual disability , fluorescence in situ hybridization , physical examination , heart disease , biology , psychiatry , chromosome , gene , biochemistry
22q11.2 deletion syndrome is one of the most prevalent microdeletion syndromes in humans. The syndrome is characterized by extensive phenotypic variability.
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