{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,14]],"date-time":"2026-08-14T19:56:01Z","timestamp":1786737361727,"version":"build-2736575974"},"reference-count":11,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"3","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Indian J Pathol Microbiol"],"published-print":{"date-parts":[[2020]]},"DOI":"10.4103\/ijpm.ijpm_465_19","type":"journal-article","created":{"date-parts":[[2020,8,24]],"date-time":"2020-08-24T03:38:12Z","timestamp":1598240292000},"page":"481","source":"Crossref","is-referenced-by-count":1,"title":["Case series of HbQ-India, a rare alpha globin variant in a referral laboratory setting in South India"],"prefix":"10.4103","volume":"63","author":[{"given":"Manu","family":"Goyal","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ayeesha","family":"Shaik","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"SreejaT","family":"Thekkelakayil","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Vijay","family":"Kumawat","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Anurag","family":"Gupta","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"276","reference":[{"key":"key-10.4103\/0377-4929.291673-1","doi-asserted-by":"crossref","first-page":"160","DOI":"10.1080\/09674845.2007.11732780","article-title":"HbQ (India) and its interaction with beta-thalassemia: A study of 64 cases from India","author":"Phanasgaonkar","year":"2007","journal-title":"Br J Biomed Sci"},{"key":"key-10.4103\/0377-4929.291673-2","doi-asserted-by":"crossref","first-page":"296","DOI":"10.1136\/jcp.56.4.296","article-title":"HbQ-India: An uncommon variant diagnosed in three Punjabi patients with diabetes is identified by a novel DNA analysis test","author":"Abraham","year":"2003","journal-title":"J Clin Pathol"},{"key":"key-10.4103\/0377-4929.291673-3","doi-asserted-by":"crossref","first-page":"436","DOI":"10.1136\/jmg.9.4.436","article-title":"Hemoglobin Q India (alpha 64 (E13) aspartic acid to histidine) associated with beta thalassemia observed in three Sindhi families","author":"Sukumaran","year":"1972","journal-title":"J Med Genet"},{"key":"key-10.4103\/0377-4929.291673-4","doi-asserted-by":"crossref","first-page":"1736","DOI":"10.1373\/clinchem.2004.034991","article-title":"HPLC Retention time as a diagnostic tool for hemoglobin variants and hemoglobinopathies: A study of 60000 samples in a clinical diagnostic laboratory","author":"Joutovsky","year":"2004","journal-title":"Clin Chem"},{"key":"key-10.4103\/0377-4929.291673-5","unstructured":"Higgs DR, Thein SL, Wood WG. Distribution and population genetics of the thalassemia's. In: Weatherall DJ, Clegg JB, editors. The Thalassaemia Syndromes. 4th ed. Oxford, England: Blackwell Scientific Publications; 2001. p. 237-84."},{"key":"key-10.4103\/0377-4929.291673-6","doi-asserted-by":"crossref","first-page":"299","DOI":"10.1007\/s12288-017-0864-2","article-title":"Clinico-hematological profile of Hb Q India: An uncommon hemoglobin variant","author":"Harrison","year":"2018","journal-title":"Indian J Hematol Blood Transfus"},{"key":"key-10.4103\/0377-4929.291673-7","doi-asserted-by":"crossref","first-page":"245","DOI":"10.1002\/ajh.20240","article-title":"Hb Q India: Is it always benign?","author":"Panigrahi","year":"2005","journal-title":"Am Hematol"},{"key":"key-10.4103\/0377-4929.291673-8","doi-asserted-by":"crossref","first-page":"117","DOI":"10.1111\/j.1365-2141.1970.tb01607.x","article-title":"Two haemoglobins Q, alpha alpha-73(EF3) and alpha-75 (EF4) aspartic acid to histidine","author":"Lorkin","year":"1970","journal-title":"Br J Haematol"},{"key":"key-10.4103\/0377-4929.291673-9","doi-asserted-by":"crossref","first-page":"91","DOI":"10.1002\/ajh.2830450116","article-title":"Quantities of alpha Q chain variants in heterozygotes with and without a concomitant beta trait","author":"Qin","year":"1994","journal-title":"Am J Hematol"},{"key":"key-10.4103\/0377-4929.291673-10","doi-asserted-by":"crossref","first-page":"487","DOI":"10.1007\/BF00484621","article-title":"Alpha-thalassemia and the production of different alpha chain variants in heterozygotes","author":"Felice","year":"1981","journal-title":"Biochem Genet"},{"key":"key-10.4103\/0377-4929.291673-11","doi-asserted-by":"crossref","first-page":"1227","DOI":"10.1007\/s00277-017-3020-z","article-title":"HbQ-India (HBA1:c.193G>C): Hematological profiles and unique CE-HPLC findings of potential diagnostic utility in 65 cases","author":"Sharma","year":"2017","journal-title":"Ann Hematol"}],"container-title":["Indian Journal of Pathology and Microbiology"],"original-title":[],"language":"en","deposited":{"date-parts":[[2026,8,14]],"date-time":"2026-08-14T18:53:26Z","timestamp":1786733606000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.ovid.com\/10.4103\/IJPM.IJPM_465_19"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2020]]},"references-count":11,"journal-issue":{"issue":"3","published-print":{"date-parts":[[2020]]}},"alternative-id":["291673"],"URL":"https:\/\/doi.org\/10.4103\/ijpm.ijpm_465_19","relation":{},"ISSN":["0377-4929"],"issn-type":[{"value":"0377-4929","type":"print"}],"subject":[],"published":{"date-parts":[[2020]]}}}