The American Cancer Society medical and editorial content team. "Family Cancer Syndromes". American Cancer Society. Archived from the original on 2013-08-02. Retrieved 2016-03-25.
Goldberg AC, Hopkins PN, Toth PP, Ballantyne CM, Rader DJ, Robinson JG, et al. (June 2011). "Familial hypercholesterolemia: screening, diagnosis and management of pediatric and adult patients: clinical guidance from the National Lipid Association Expert Panel on Familial Hypercholesterolemia". Journal of Clinical Lipidology. 5 (3 Suppl): S1-8. doi:10.1016/j.jacl.2011.04.003. PMID21600525.
Gidding SS, Champagne MA, de Ferranti SD, Defesche J, Ito MK, Knowles JW, et al. (December 2015). "The Agenda for Familial Hypercholesterolemia: A Scientific Statement From the American Heart Association". Circulation. 132 (22): 2167–92. doi:10.1161/CIR.0000000000000297. PMID26510694. S2CID9980924.
Pong AW, Pal DK, Chung WK (May 2011). "Developments in molecular genetic diagnostics: an update for the pediatric epilepsy specialist". Pediatric Neurology. 44 (5): 317–27. doi:10.1016/j.pediatrneurol.2011.01.017. PMID21481738.
Helbig I, Scheffer IE, Mulley JC, Berkovic SF (March 2008). "Navigating the channels and beyond: unravelling the genetics of the epilepsies". The Lancet. Neurology. 7 (3): 231–45. doi:10.1016/S1474-4422(08)70039-5. PMID18275925. S2CID23243066.
Crozier S, Robertson N, Dale M (February 2015). "The psychological impact of predictive genetic testing for Huntington's disease: a systematic review of the literature". Journal of Genetic Counseling. 24 (1): 29–39. doi:10.1007/s10897-014-9755-y. PMID25236481. S2CID18140209.
American College of Obstetricians Gynecologists' Committee on Practice Bulletins—Obstetrics; Society for Maternal–Fetal Medicine (May 2016). "Practice Bulletin No. 162: Prenatal Diagnostic Testing for Genetic Disorders". Obstetrics and Gynecology. 127 (5): e108–e122. doi:10.1097/AOG.0000000000001405. PMID26938573. S2CID25791506.
Benn P, Borrell A, Chiu RW, Cuckle H, Dugoff L, Faas B, et al. (August 2015). "Position statement from the Chromosome Abnormality Screening Committee on behalf of the Board of the International Society for Prenatal Diagnosis". Prenatal Diagnosis. 35 (8): 725–34. doi:10.1002/pd.4608. PMID25970088. S2CID23477914.
Wilson KL, Czerwinski JL, Hoskovec JM, Noblin SJ, Sullivan CM, Harbison A, et al. (February 2013). "NSGC practice guideline: prenatal screening and diagnostic testing options for chromosome aneuploidy". Journal of Genetic Counseling. 22 (1): 4–15. doi:10.1007/s10897-012-9545-3. PMID23179172. S2CID13126623.
Committee On Practice Bulletins—Obstetrics; Committee on Genetics (May 2016). "Practice Bulletin No. 163: Screening for Fetal Aneuploidy". Obstetrics and Gynecology. 127 (5): e123–e137. doi:10.1097/AOG.0000000000001406. PMID26938574. S2CID40095460.
"Committee Opinion No. 690 Summary: Carrier Screening in the Age of Genomic Medicine". Obstetrics and Gynecology. 129 (3): 595–596. March 2017. doi:10.1097/AOG.0000000000001947. PMID28225420.
Tsuang MT (December 1978). "Genetic counseling for psychiatric patients and their families". The American Journal of Psychiatry. 135 (12): 1465–75. doi:10.1176/ajp.135.12.1465. PMID717559.
Halbert CH, Harrison BW (March 2018). "Genetic counseling among minority populations in the era of precision medicine". American Journal of Medical Genetics. Part C, Seminars in Medical Genetics. 178 (1): 68–74. doi:10.1002/ajmg.c.31604. PMID29575517. S2CID4325950.
Goldberg AC, Hopkins PN, Toth PP, Ballantyne CM, Rader DJ, Robinson JG, et al. (June 2011). "Familial hypercholesterolemia: screening, diagnosis and management of pediatric and adult patients: clinical guidance from the National Lipid Association Expert Panel on Familial Hypercholesterolemia". Journal of Clinical Lipidology. 5 (3 Suppl): S1-8. doi:10.1016/j.jacl.2011.04.003. PMID21600525.
Gidding SS, Champagne MA, de Ferranti SD, Defesche J, Ito MK, Knowles JW, et al. (December 2015). "The Agenda for Familial Hypercholesterolemia: A Scientific Statement From the American Heart Association". Circulation. 132 (22): 2167–92. doi:10.1161/CIR.0000000000000297. PMID26510694. S2CID9980924.
Pong AW, Pal DK, Chung WK (May 2011). "Developments in molecular genetic diagnostics: an update for the pediatric epilepsy specialist". Pediatric Neurology. 44 (5): 317–27. doi:10.1016/j.pediatrneurol.2011.01.017. PMID21481738.
Helbig I, Scheffer IE, Mulley JC, Berkovic SF (March 2008). "Navigating the channels and beyond: unravelling the genetics of the epilepsies". The Lancet. Neurology. 7 (3): 231–45. doi:10.1016/S1474-4422(08)70039-5. PMID18275925. S2CID23243066.
Crozier S, Robertson N, Dale M (February 2015). "The psychological impact of predictive genetic testing for Huntington's disease: a systematic review of the literature". Journal of Genetic Counseling. 24 (1): 29–39. doi:10.1007/s10897-014-9755-y. PMID25236481. S2CID18140209.
American College of Obstetricians Gynecologists' Committee on Practice Bulletins—Obstetrics; Society for Maternal–Fetal Medicine (May 2016). "Practice Bulletin No. 162: Prenatal Diagnostic Testing for Genetic Disorders". Obstetrics and Gynecology. 127 (5): e108–e122. doi:10.1097/AOG.0000000000001405. PMID26938573. S2CID25791506.
Benn P, Borrell A, Chiu RW, Cuckle H, Dugoff L, Faas B, et al. (August 2015). "Position statement from the Chromosome Abnormality Screening Committee on behalf of the Board of the International Society for Prenatal Diagnosis". Prenatal Diagnosis. 35 (8): 725–34. doi:10.1002/pd.4608. PMID25970088. S2CID23477914.
Wilson KL, Czerwinski JL, Hoskovec JM, Noblin SJ, Sullivan CM, Harbison A, et al. (February 2013). "NSGC practice guideline: prenatal screening and diagnostic testing options for chromosome aneuploidy". Journal of Genetic Counseling. 22 (1): 4–15. doi:10.1007/s10897-012-9545-3. PMID23179172. S2CID13126623.
Committee On Practice Bulletins—Obstetrics; Committee on Genetics (May 2016). "Practice Bulletin No. 163: Screening for Fetal Aneuploidy". Obstetrics and Gynecology. 127 (5): e123–e137. doi:10.1097/AOG.0000000000001406. PMID26938574. S2CID40095460.
"Committee Opinion No. 690 Summary: Carrier Screening in the Age of Genomic Medicine". Obstetrics and Gynecology. 129 (3): 595–596. March 2017. doi:10.1097/AOG.0000000000001947. PMID28225420.
Tsuang MT (December 1978). "Genetic counseling for psychiatric patients and their families". The American Journal of Psychiatry. 135 (12): 1465–75. doi:10.1176/ajp.135.12.1465. PMID717559.
Halbert CH, Harrison BW (March 2018). "Genetic counseling among minority populations in the era of precision medicine". American Journal of Medical Genetics. Part C, Seminars in Medical Genetics. 178 (1): 68–74. doi:10.1002/ajmg.c.31604. PMID29575517. S2CID4325950.
Gidding SS, Champagne MA, de Ferranti SD, Defesche J, Ito MK, Knowles JW, et al. (December 2015). "The Agenda for Familial Hypercholesterolemia: A Scientific Statement From the American Heart Association". Circulation. 132 (22): 2167–92. doi:10.1161/CIR.0000000000000297. PMID26510694. S2CID9980924.
Helbig I, Scheffer IE, Mulley JC, Berkovic SF (March 2008). "Navigating the channels and beyond: unravelling the genetics of the epilepsies". The Lancet. Neurology. 7 (3): 231–45. doi:10.1016/S1474-4422(08)70039-5. PMID18275925. S2CID23243066.
Crozier S, Robertson N, Dale M (February 2015). "The psychological impact of predictive genetic testing for Huntington's disease: a systematic review of the literature". Journal of Genetic Counseling. 24 (1): 29–39. doi:10.1007/s10897-014-9755-y. PMID25236481. S2CID18140209.
American College of Obstetricians Gynecologists' Committee on Practice Bulletins—Obstetrics; Society for Maternal–Fetal Medicine (May 2016). "Practice Bulletin No. 162: Prenatal Diagnostic Testing for Genetic Disorders". Obstetrics and Gynecology. 127 (5): e108–e122. doi:10.1097/AOG.0000000000001405. PMID26938573. S2CID25791506.
Benn P, Borrell A, Chiu RW, Cuckle H, Dugoff L, Faas B, et al. (August 2015). "Position statement from the Chromosome Abnormality Screening Committee on behalf of the Board of the International Society for Prenatal Diagnosis". Prenatal Diagnosis. 35 (8): 725–34. doi:10.1002/pd.4608. PMID25970088. S2CID23477914.
Wilson KL, Czerwinski JL, Hoskovec JM, Noblin SJ, Sullivan CM, Harbison A, et al. (February 2013). "NSGC practice guideline: prenatal screening and diagnostic testing options for chromosome aneuploidy". Journal of Genetic Counseling. 22 (1): 4–15. doi:10.1007/s10897-012-9545-3. PMID23179172. S2CID13126623.
Committee On Practice Bulletins—Obstetrics; Committee on Genetics (May 2016). "Practice Bulletin No. 163: Screening for Fetal Aneuploidy". Obstetrics and Gynecology. 127 (5): e123–e137. doi:10.1097/AOG.0000000000001406. PMID26938574. S2CID40095460.
Halbert CH, Harrison BW (March 2018). "Genetic counseling among minority populations in the era of precision medicine". American Journal of Medical Genetics. Part C, Seminars in Medical Genetics. 178 (1): 68–74. doi:10.1002/ajmg.c.31604. PMID29575517. S2CID4325950.
"Course". University of Technology Sydney. Retrieved 2024-02-21.
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The American Cancer Society medical and editorial content team. "Family Cancer Syndromes". American Cancer Society. Archived from the original on 2013-08-02. Retrieved 2016-03-25.