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The Application of Clinical Genetics
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The Application of Clinical Genetics
(588,105) Views
Editor in Chief Martin Henrik Maurer
1178-704X
ReviewDisorders caused by chromosome abnormalities
Aaron Theisen, Lisa G Shaffer
The Application of Clinical Genetics 2010, 3:159-174
10 December 2010
Review
Genetic screening for homozygous and heterozygous familial hypercholesterolemia
Maria C Izar, Valéria A Machado, Francisco A Fonseca
The Application of Clinical Genetics 2010, 3:147-157
08 December 2010
Review
Recent developments in the treatment of acute abdominal and facial attacks of hereditary angioedema: focus on human C1 esterase inhibitor
Lourdes Pastó Cardona, Ramon Lleonart Bellfill, Joaquim Marcoval Caus
The Application of Clinical Genetics 2010, 3:133-146
03 December 2010
Review
Management of the asymptomatic BRCA mutation carrier
Paige Teller, Rita K Kramer
The Application of Clinical Genetics 2010, 3:121-131
24 November 2010
Review
Allergic rhinitis and genetic components: focus on Toll-like receptors (TLRs) gene polymorphism
Zhiwei Gao, Donna C Rennie, Ambikaipakan Senthilselvan
The Application of Clinical Genetics 2010, 3:109-120
16 November 2010
Review
Psychogenetics of post-traumatic stress disorder: a short review
Ahmed Rady, Adel Elsheshai, Osama Elkholy, et al
The Application of Clinical Genetics 2010, 3:103-108
16 November 2010
Review
Diagnostic criteria, specific mutations, and genetic predisposition in gastrointestinal stromal tumors
Jean-Baptiste Bachet, Jean-François Emile
The Application of Clinical Genetics 2010, 3:85-101
29 October 2010
Review
Genetic contribution and associated pathophysiology in end-stage renal disease
Suraksha Agrawal, SS Agarwal, Sita Naik
The Application of Clinical Genetics 2010, 3:65-84
05 August 2010
Review
The genetic basis of familial hypercholesterolemia: inheritance, linkage, and mutations
Isabel De Castro-Orós, Miguel Pocoví, Fernando Civeira
The Application of Clinical Genetics 2010, 3:53-64
05 August 2010
Review
Genetic and molecular mechanisms in multiple myeloma: a route to better understand disease pathogenesis and heterogeneity
Marie-Christine Kyrtsonis, Vassiliki Bartzis, Xenophon Papanikolaou, et al
The Application of Clinical Genetics 2010, 3:41-51
28 July 2010
Original Research
Congenital malformations in Ecuadorian children: urgent need to create a National Registry of Birth Defects
Fabricio González-Andrade, Ramiro López-Pulles
The Application of Clinical Genetics 2010, 3:29-39
14 April 2010
Original Research
Gene polymorphisms in association with self-reported stroke in US adults
Amy Z Fan, Jing Fang, Ajay Yesupriya, et al
The Application of Clinical Genetics 2010, 3:23-28
11 March 2010
Original Research
Pilot study of an association between a common variant in the non-muscle myosin heavy chain 9 (MYH9) gene and type 2 diabetic nephropathy in a Taiwanese population
Chang-Hsun Hsieh, Yi-Jen Hung, Dee Pei, et al
The Application of Clinical Genetics 2010, 3:17-22
16 March 2010
Other
Amniotic band syndrome and/or limb body wall complex: split or lump
Ashutosh Halder
The Application of Clinical Genetics 2010, 3:7-15
04 February 2010
Original Research
Inheritance of craniofacial features in Colombian families with class III malocclusion
L Otero, L Quintero, D Champsaur, et al
The Application of Clinical Genetics 2010, 3:1-6
03 February 2010
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