(2012). The Use of Intron 22 Mutation in Detection of Haemophilia A Carrier in Patient's Siblings. test, 15(04.2012), 0-0. doi: 10.21608/jsc.2012.62926
. "The Use of Intron 22 Mutation in Detection of Haemophilia A Carrier in Patient's Siblings". test, 15, 04.2012, 2012, 0-0. doi: 10.21608/jsc.2012.62926
(2012). 'The Use of Intron 22 Mutation in Detection of Haemophilia A Carrier in Patient's Siblings', test, 15(04.2012), pp. 0-0. doi: 10.21608/jsc.2012.62926
The Use of Intron 22 Mutation in Detection of Haemophilia A Carrier in Patient's Siblings. test, 2012; 15(04.2012): 0-0. doi: 10.21608/jsc.2012.62926

The Use of Intron 22 Mutation in Detection of Haemophilia A Carrier in Patient's Siblings

مجلة دراسات الطفولة
Article 14, Volume 15, Issue 04.2012, April 2012, Pages 0-0    PDF (3.2 M)
Document Type: المقالة الأصلية
DOI: 10.21608/jsc.2012.62926
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