نتائج البحث

CDKN2A genetic testing in melanoma-prone families in Sweden in the years 2015–2020: implications for novel national recommendations.

• Authors : Pissa, Maria¹; Helkkula, Teo^2,3; Appelqvist, Frida⁴

• Source: Acta Oncologica. Jul2021, Vol. 60 Issue 7, p888-896. 9p. 5 Charts, 1 Map.

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A geographically matched control population efficiently limits the number of candidate disease-causing variants in an unbiased whole-genome analysis.

• Authors : Rentoft, Matilda^1,2; Svensson, Daniel²; Sjödin, Andreas^2,3

Subjects: *BIRTH control; *GENETIC disorders; *COLON cancerEUROPE; SWEDEN

• Source: PLoS ONE. 3/27/2019, Vol. 14 Issue 3, p1-17. 17p.

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Genetic anticipation in Swedish Lynch syndrome families.

• Authors : von Salomé, Jenny¹ ; Boonstra, Philip S.²; Karimi, Masoud³

• Source: PLoS Genetics. 10/31/2017, Vol. 13 Issue 11, p1-13. 13p.

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Novel mutations in CRB1 and ABCA4 genes cause Leber congenital amaurosis and Stargardt disease in a Swedish family.

• Authors : Jonsson, Frida¹; Burstedt, Marie S²; Sandgren, Ola²

• Source: European Journal of Human Genetics. Nov2013, Vol. 21 Issue 11, p1266-1271. 6p.

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Age of onset in familial breast cancer as background data for medical surveillance.

• Authors : Brandt, A.¹ ; Bermejo, J. Lorenzo^1,2; Sundquist, J.^3,4

• Source: British Journal of Cancer. 1/4/2010, Vol. 102 Issue 1, p42-47. 6p. 3 Charts, 1 Graph.

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Norrbottnian congenital insensitivity to pain.

• Authors : Minde, Jan K.

• Source: Acta Orthopaedica (Supplement). Apr2006 Supplement 321, Vol. 77, preceding p1-32. 33p. 6 Color Photographs, 3 Diagrams, 9 Charts, 1 Graph, 1 Map.

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Familial association between type 1 diabetes and other autoimmune and related diseases.

• Authors : Hemminki K; Division of Molecular Genetic Epidemiology, German Cancer Research Center (DKFZ), Im Neuenheimer Feld 580, 69120, Heidelberg, Germany. ; Li X

Subjects: Autoimmune Diseases/Autoimmune Diseases/Autoimmune Diseases/*genetics ; Diabetes Mellitus, Type 1/Diabetes Mellitus, Type 1/Diabetes Mellitus, Type 1/*genetics; Adolescent

• Source: Diabetologia [Diabetologia] 2009 Sep; Vol. 52 (9), pp. 1820-8. Date of Electronic Publication: 2009 Jun 20.Publisher: Springer Verlag Country of Publication: Germany NLM ID: 0006777 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Norrbottnian congenital insensitivity to pain.

• Authors : Minde JK; Department of Orthopedics, Gällivare Hospital, Gällivare, Sweden.

Subjects: Mutation*; Genetic Predisposition to Disease/Genetic Predisposition to Disease/Genetic Predisposition to Disease/*epidemiology ; Nerve Growth Factors/Nerve Growth Factors/Nerve Growth Factors/*genetics

• Source: Acta orthopaedica. Supplementum [Acta Orthop Suppl] 2006 Apr; Vol. 77 (321), pp. 2-32.Publisher: Taylor & Francis Country of Publication: Sweden NLM ID: 101244827 Publication Model: Print Cited Medium: Print

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