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Di laman Talasemia:
"Kedua-dua talasemia α- dan β sering diwarisi secara autosomal resesif. Kes talasemia α- dan β yang diwarisi secara dominan telah dilaporkan, yang pertama adalah dalam keluarga Ireland dengan dua penghapusan 4 dan 11 bp dalam exon 3 diganggu oleh penyisipan 5 bp dalam gen β-globin. Untuk bentuk penyakit resesif autosomal, kedua-dua ibu bapa mesti menjadi pembawa untuk kanak-kanak yang terjejas. Jika kedua-dua ibu bapa mempunyai sifat hemoglobinopati, risikonya ialah 25% bagi setiap kehamilan untuk anak yang terjejas.[perlu rujukan]
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