Hemoglobin H (Hb H) disease in Canada: molecular diagnosis and review of 116 cases.
about
Clinical and molecular analysis of haemoglobin H disease in Sardinia: haematological, obstetric and cardiac aspects in patients with different genotypesHb H hydrops foetalis syndrome: a case report and review of literature.A review of the molecular diagnosis of thalassemia.Hemoglobin H disease in Muscat, Oman - A 5 year studyA laboratory strategy for genotyping haemoglobin H disease in the Chinese.Hematological Analysis in Thai Samples With Deletional and Nondeletional HbH Diseases.Validation of a reverse-hybridization StripAssay for the simultaneous analysis of common alpha-thalassemia point mutations and deletions.
P2860
Q28275797-D33FF785-DD71-4B3A-BBAD-89740C40EA2CQ34448336-8A8C0443-9276-4B5A-A5A7-1859B3389A0DQ35670977-023271D3-42F3-4865-973B-4289B01840DAQ35765429-A4B08D2B-F39F-4631-A5D4-649F282F2DD1Q41385863-CAD1DE7A-DC7A-4412-9972-61F49C041E6EQ49963703-2D429081-F306-49C1-8C05-6AA32C812DA8Q51010490-B7D53BC1-FD6E-43FB-BB51-FC13D1D718EA
P2860
Hemoglobin H (Hb H) disease in Canada: molecular diagnosis and review of 116 cases.
description
2001 nî lūn-bûn
@nan
2001 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
name
Hemoglobin H (Hb H) disease in Canada: molecular diagnosis and review of 116 cases.
@ast
Hemoglobin H (Hb H) disease in Canada: molecular diagnosis and review of 116 cases.
@en
Hemoglobin H
@nl
type
label
Hemoglobin H (Hb H) disease in Canada: molecular diagnosis and review of 116 cases.
@ast
Hemoglobin H (Hb H) disease in Canada: molecular diagnosis and review of 116 cases.
@en
Hemoglobin H
@nl
prefLabel
Hemoglobin H (Hb H) disease in Canada: molecular diagnosis and review of 116 cases.
@ast
Hemoglobin H (Hb H) disease in Canada: molecular diagnosis and review of 116 cases.
@en
Hemoglobin H
@nl
P2093
P2860
P356
P1476
Hemoglobin H (Hb H) disease in Canada: molecular diagnosis and review of 116 cases.
@en
P2093
Olivieri NF
Patterson M
P2860
P356
10.1002/AJH.1142
P577
2001-09-01T00:00:00Z