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تقرير مؤتمر أسبانيا: التخطيط الإستراتيجي للمشروع العالمي للفاريوم البشري Planning the Human Variome Project: The Spain Report
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Article In Journal |
2009 |
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تحليل الطفرة الجينية في متلازمة دوشين وبيكر للضمور العضلي باستخدام PCR Mutation analysis in Saudi Duchenne and Becker muscular dystrophy patients using multiplex PCR..
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Article In Journal |
2008 |
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الأمـراض الوراثية والعيوب الخلقية التـي تصيـب الفك و الأسنان Clinical genetics: Practical applications for dentists and oral surgeons
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2008 |
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" مدى إدراك طلبة جامعة الملك عبد العزيز بجدة بمفاهيم الفحص المبكر قبل الزواج في المملكة العربية السعودية "Knowledge regarding the national premarital screening program among university students in Jeddah, Kingdom of Saudi Arabia"
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2008 |
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نسبة انتشار العامل V Leiden والطفرة الجينية G20210Aلتخثر الدم. Correspondence re: Prevalence of factor V Leiden and prothrombin G20210A gene mutation
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Article In Journal |
2005 |
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التواء الخصية Testicular Torsion: An Antenatal Event
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Article In Journal |
2002 |
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هل يمكن خفض معدل الإصابة بالتشنجات المتواصلة؟ Status Epilepticus: Can the Incidence be Reduced?
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Article In Journal |
2002 |
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A newly described mutation of the CLCN7 gene causes neuropathic autosomal recessive osteopetrosis in an Arab family A newly described mutation of the CLCN7 gene causes neuropathic autosomal recessive osteopetrosis in an Arab family
Lippincott, Williams & Wilkins |
Article In Journal |
1433 |
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Recommendations for genetic variation data capture in developing countries to ensure a comprehensive worldwide data collection Recommendations for genetic variation data capture in developing countries to ensure a comprehensive worldwide data collection
Human Genome Variation Society |
Article In Journal |
1432 |
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How to catch all those mutations--the report of the third Human Variome Project Meeting, UNESCO Paris, May 2010 How to catch all those mutations--the report of the third Human Variome Project Meeting, UNESCO Paris, May 2010
Human Genome Variation Society |
Article In Journal |
1432 |
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Mutations in the pre-replication complex cause Meier-Gorlin syndrome Mutations in the pre-replication complex cause Meier-Gorlin syndrome
Nature Publishing Group |
Article In Journal |
1432 |
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Initiating a Human Variome Project Country Node Initiating a Human Variome Project Country Node
Human Genome Variation Society |
Article In Journal |
1432 |
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Attitudes towards mandatory national premarital screening for hereditary hemolytic disorders Attitudes towards mandatory national premarital screening for hereditary hemolytic disorders
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Article In Journal |
1431 |
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Planning the Human Variome Project: The Spain Report Planning the Human Variome Project: The Spain Report
Human Genome Variation Society |
Article In Journal |
1430 |
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طفرات فقد الوظائف في جين ا ت ب6ف0ا2 يضعف المرور الحويصلي وترسب الايلاستين وبقاء الخلايا LOSS-OF-FUNCTION MUTATIONS IN ATP6V0A2 IMPAIR VESICULAR TRAFFICKING, ELASTIN DEPOSITION, AND CELL SURVIVAL
Oxford Journals |
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1430 |
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CLINICAL GENETICS: PRACTICAL APPLICATIONS FOR DENTISTS’ AND ORAL SURGEONS CLINICAL GENETICS: PRACTICAL APPLICATIONS FOR DENTISTS’ AND ORAL SURGEONS
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Article In Journal |
1429 |
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A prospective study of congenital malformations among live born neonates at University Hospital in Western Saudi Arabia A prospective study of congenital malformations among live born neonates at University Hospital in Western Saudi Arabia
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1428 |
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Pattern of infant feeding at a University Hospital in Western Saudi Arabia Pattern of infant feeding at a University Hospital in Western Saudi Arabia
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Article In Journal |
1424 |
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Status epilepticus Can the incidence be reduced ? Status epilepticus Can the incidence be reduced ?
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Article In Journal |
1423 |
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