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British Journal of Haematology|February 1, 1997
Molecular defects in Hb H hydrops fetalisV Chan, V W Chan, M Tang, et al.Prenatal Diagnosis|October 1, 1993
False non-paternity in a family for prenatal diagnosis of beta-thalassaemiaV Chan, T P Chan, K Lau, et al.Blood|October 1, 1988
A novel beta-thalassemia frameshift mutation (codon 14/15), detectable by direct visualization of abnormal restriction fragment in amplified genomic DNAV Chan, T K Chan, Y W Kan, et al.American Journal of Hematology|March 1, 1987
Combination of three alpha-globin gene loci deletions and hemoglobin New York results in a severe hemoglobin H syndromeV Chan, T K Chan, S C Tso, et al.American Journal of Human Genetics|October 1, 1987
Distribution of beta-thalassemia mutations in south China and their association with haplotypesV Chan, T K Chan, F F Chebab, et al.Blood|December 1, 1989
A novel missense mutation in exon 4 of the factor VIII:C gene resulting in moderately severe hemophilia AV Chan, T K Chan, T M Tong, et al.American Journal of Hematology|May 20, 1998
Hemophilia B in a female carrier due to skewed inactivation of the normal X-chromosomeV Chan, V W Chan, B Yip, et al.British Journal of Haematology|May 1, 1996
Molecular characterization of haemophilia A in southern ChineseV Chan, A Pang, T P Chan, et al.Hematological Oncology|May 1, 1992
Detection of immunoglobulin gene rearrangement in B-cell lymphomas by polymerase chain reaction gene amplificationR Liang, V Chan, T K Chan, et al.Pageof 473