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Academic Journal

Detecting rare thalassemia in children with anemia using third-generation sequencing.

Authors : Ren, Zhen-min¹ (AUTHOR); Li, Wu-jiao¹ (AUTHOR); Xing, Zhi-hao¹ (AUTHOR)

Source: Hematology. Dec2023, Vol. 28 Issue 1, p1-5. 5p.

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Academic Journal

Diversity and Classification of Genetic Variations in Autism Spectrum Disorder.

Authors : Kereszturi, Éva¹ (AUTHOR)

Source: International Journal of Molecular Sciences. Dec2023, Vol. 24 Issue 23, p16768. 20p.

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Academic Journal

Physicians' use and perceptions of genetic testing for rare diseases in China: a nationwide cross-sectional study.

Authors : Liu, Weida¹ (AUTHOR); Liu, Peng¹ (AUTHOR); Guo, Dan² (AUTHOR)

Source: Orphanet Journal of Rare Diseases. 8/10/2023, Vol. 18 Issue 1, p1-9. 9p.

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Academic Journal

An Overview of Pancreatic Neuroendocrine Tumors and an Update on Endoscopic Techniques for Their Management.

Authors : Elkelany, Osama O.¹ (AUTHOR); Karaisz, Fred G.² (AUTHOR); Davies, Benjamin³ (AUTHOR)

Source: Current Oncology. Aug2023, Vol. 30 Issue 8, p7566-7580. 15p. 6 Charts.

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Academic Journal

GENETİK ŞƏRTLƏNMİŞ XƏSTƏLİKLƏRİN EPİDEMİOLOJİ XARAKTERİSTİKASI.

Authors : Ağayev, İbadulla¹ ; Xələfli, Xatirə² ; Niftullayev, Məhərrəm¹

Source: Nature & Science / Təbiət və Elm. 2023, Vol. 5 Issue 7, p7-12. 6p.

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Academic Journal

Psychosocial factors impacting barriers and motivators to cancer genetic testing.

Authors : Hanson, Erika N.¹ (AUTHOR) ; Delacroix, Emerson² (AUTHOR); Austin, Sarah¹ (AUTHOR)

Source: Cancer Medicine. Apr2023, Vol. 12 Issue 8, p9945-9955. 11p.

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Academic Journal

Dietitians' and nutritionists' knowledge of nutritional genomics and perception toward genetic testing for a personalized approach in noncommunicable diseases (NCDs) prevention and management in India: A cross-sectional survey.

Authors : Mathew, Mary Raju¹; Medithi, Srujana¹ ; Muley, Arti¹

Source: International Journal of Nutrition, Pharmacology, Neurological Diseases. Apr-Jun2023, Vol. 13 Issue 2, p123-131. 9p.

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Academic Journal

The importance of direct genetic testing for determining female carriers of the mutation in dystrophinopathies.

Authors : Maksić, Jasmina¹; Maksimović, Nela²; Rasulić, Lukas^2,3

Source: Vojnosanitetski Pregled: Military Medical & Pharmaceutical Journal of Serbia. Mar2023, Vol. 80 Issue 3, p201-207. 7p.

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Academic Journal

The Michigan Genetic Hereditary Testing (MiGHT) study's innovative approaches to promote uptake of clinical genetic testing among cancer patients: a study protocol for a 3-arm randomized controlled trial.

Authors : Gerido, Lynette Hammond¹ (AUTHOR) ; Griggs, Jennifer J.^1,2,3 (AUTHOR); Resnicow, Ken^1,2 (AUTHOR)

Source: Trials. 2/10/2023, Vol. 24 Issue 1, p1-13. 13p. 2 Charts.

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Academic Journal

Fatalism and metaphor in Confucianism: A qualitative study of barriers to genetic testing among first‐degree relatives of hereditary cancer patients from China.

Authors : Jiang, Chaonan¹ (AUTHOR); Liu, Li¹ (AUTHOR); Wang, Ye¹ (AUTHOR)

Source: Psycho-Oncology. Feb2023, Vol. 32 Issue 2, p275-282. 8p. 1 Chart.

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نتائج البحث

فلترة النتائج

Detecting rare thalassemia in children with anemia using third-generation sequencing.

Diversity and Classification of Genetic Variations in Autism Spectrum Disorder.

Physicians' use and perceptions of genetic testing for rare diseases in China: a nationwide cross-sectional study.

An Overview of Pancreatic Neuroendocrine Tumors and an Update on Endoscopic Techniques for Their Management.

GENETİK ŞƏRTLƏNMİŞ XƏSTƏLİKLƏRİN EPİDEMİOLOJİ XARAKTERİSTİKASI.

Psychosocial factors impacting barriers and motivators to cancer genetic testing.

Dietitians' and nutritionists' knowledge of nutritional genomics and perception toward genetic testing for a personalized approach in noncommunicable diseases (NCDs) prevention and management in India: A cross-sectional survey.

The importance of direct genetic testing for determining female carriers of the mutation in dystrophinopathies.

The Michigan Genetic Hereditary Testing (MiGHT) study's innovative approaches to promote uptake of clinical genetic testing among cancer patients: a study protocol for a 3-arm randomized controlled trial.

Fatalism and metaphor in Confucianism: A qualitative study of barriers to genetic testing among first‐degree relatives of hereditary cancer patients from China.

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