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1.
Thalassemia in Western Australia: 11 novel deletions characterized by Multiplex Ligation-dependent Probe Amplification.
Blood Cells Mol Dis
; 44(3): 146-51, 2010 Mar 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-20110179
2.
Two new alpha1-globin gene point mutations: Hb Nedlands (HBA1:c.86C>T) [alpha28(B9)Ala-->Val] and Hb Queens Park (HBA1:c.98T>A) [alpha32(B13)Met-->Lys].
Hemoglobin
; 34(2): 123-6, 2010 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-20353346
3.
A moderately severe alpha-thalassemia condition resulting from a combination of the alpha2 polyadenylation signal (AATAAA-->AATA- -) mutation and a 3.7 Kb alpha gene deletion in an Australian family.
Hemoglobin
; 31(2): 173-7, 2007.
Artículo
en Inglés
| MEDLINE | ID: mdl-17486499
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