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Results for
""Genetic Carrier Screening""[mesh_terms]

61 Results

Searching titles within these results

Borderline HbA levels: Dilemma in diagnosis of beta-thalassemia carriers.

Stacy Colaco, Anita Nadkarni

Mutation research. Reviews in mutation research 2021;788():108387

The genetics of host resistance and susceptibility to tuberculosis.

P Davies, J Grange

Annals of the New York Academy of Sciences 2002;953():151-6

Genetic hemochromatosis: detection, management, and population screening.

A P Walker, J S Dooley

Genetic testing 2000;4(2):97-101

Evaluation of clinical application of gap-PCR as a routine method for alpha-thalassemia carrier detection.

Lan-Fang Zhu, Zhong-Ying Liu, Wen-Dian Li, Li-Yan Li, Ge-Fei Xiao, Yu-Qiu Zhou, Xiang-Min Xu, Xin-Jun Qu, Qiu-Hua Mo

Di 1 jun yi da xue xue bao = Academic journal of the first medical college of PLA 2002;22(5):434-6

Cystic fibrosis newborn screening: a pilot study to maximize carrier screening.

Erin Lagoe, Georgianne Arnold, Peter T Rowley, Sandra Labella

Genetic testing 2006;9(3):255-60

Expanded carrier screening in the United States: A systematic evidence review exploring client and provider experiences.

Aarti Ramdaney, Lauren Lichten, Lauren Propst, Caitlin Mann, Gabriel A Lazarin, Malorie Jones, Amy Taylor, Jennifer Malinowski

Journal of genetic counseling 2022;31(4):937-948

Genetics of idiopathic dilated cardiomyopathy.

A Pilotto, L Tavazzi, A Gavazzi, P Morbini, E Arbustini

Herz 2000;25(3):156-60

Laboratory diagnosis of thalassemia.

M D Cappellini, V Brancaleoni, E Di Pierro, I Motta

International journal of laboratory hematology 2017;38 Suppl 1():32-40

Liver transplant combined with heart transplant in severe heterozygous hypercholesterolemia: report of the first case and review of the literature.

A Khayat, J P Deshayes, A Lepage, E Saloux, Y Reznik, B J Alkofer, L Chiche

Transplantation proceedings 2005;37(5):2250-2

Update on newborn screening for cystic fibrosis.

Jeffrey S Wagener, Marci K Sontag, Scott D Sagel, Frank J Accurso

Current opinion in pulmonary medicine 2005;10(6):500-4

Beta-thalassemia.

Renzo Galanello, Antonio Cao

Genetics in medicine : official journal of the American College of Medical Genetics 2010;12(2):61-76

Thalassaemia control in developing countries--the Sri Lankan perspective.

D M Perera, M Petrou, A Wijekoon, D Gunasekara

The Ceylon medical journal 2000;45(1):12-6

Role of phosphatidylcholine-DHA in preventing APOE4-associated Alzheimer's disease.

Rhonda P Patrick

FASEB journal : official publication of the Federation of American Societies for Experimental Biology 2019;33(2):1554-1564

Plain Language Summary

Compound heterozygous mutations P336L and I1660V in the human cardiac sodium channel associated with the Brugada syndrome.

Jonathan M Cordeiro, Hector Barajas-Martinez, Kui Hong, Elena Burashnikov, Ryan Pfeiffer, Anne-Marie Orsino, Yue Sheng Wu, Dan Hu, Josep Brugada, Pedro Brugada, Charles Antzelevitch, Robert Dumaine, Ramon Brugada

Circulation 2006;114(19):2026-33

DHCR7 and Smith-Lemli-Opitz syndrome.

M J Nowaczyk, L M Nakamura, J S Waye

Clinical and investigative medicine. Medecine clinique et experimentale 2002;24(6):311-7

Results: 1 – 15 / 61

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