Clinical Genetics Virtual Issues
Clinical Genetics
- Clinical Genetics - Reviews, January 2010
- Developmental Biology February 2008
- Social and Behavioural Research February 2008
TopClinical Genetics - Reviews, January 2010
Edited by Michael R. Hayden
Read the top 10 reviews published in Clinical Genetics in 2008 and 2009 FREE
Dyskeratosis congenita: a genetic disorder of many faces
Kirwan, M; Dokal, I
Genetic heterogeneity of autosomal dominant hypercholesterolemia
Varret, M; Abifadel, M; Rabes, JP; Boileau, C
Restless legs syndrome: an update on genetics and future perspectives
Pichler, I; Hicks, AA; Pramstaller, PP
Synpolydactyly: clinical and molecular advances
Malik, S; Grzeschik, KH
MicroRNAs show a wide diversity of expression profiles in the developing and mature central nervous system
Erson, AE; Petty, EM
Inverted duplications deletions: underdiagnosed rearrangements??
Zuffardi, O; Bonaglia, M; Ciccone, R; Giorda, R
Noncoding RNAs in mental retardation
Szulwach, KE; Jin, P; Alisch, RS
Importance of gene-environment interactions in the etiology of selected birth defects
Zhu, H; Kartiko, S; Finnell, RH
Cornelia de Lange syndrome, cohesin, and beyond
Liu, J; Krantz, ID
MicroRNA epigenetic alterations: predicting biomarkers and therapeutic targets in human diseases
Wang, Y; Liang, Y; Lu, Q
TopDevelopmental Biology February 2008
Homeobox genes in vertebrate forebrain development and disease
Jeffrey Wigle, David Eisenstat
Skeletal Dysplasias and the growth plate
Benjamin Alman
Lissencephaly and LIS1: insights into the molecular mechanisms of neuronal migration and development
Anthony Wynshaw-Boris
Of Old And New Diseases: Genetics Of Pituitary Acth Excess (Cushing) And Deficiency
Jacques Drouin, Steve Bilodeau, Sophie Vallette
Development of cortical GABAergic circuits and its implications for neurodevelopmental disorders
Graziella Di Cristo
Towards understanding the genetic basis of neural tube defects
Zoha Kibar, Valeria Capra, Philippe Gros
Gene discovery in craniofacial development and disease - cashing in your chips
G R Handrigan, M Buchtova, Joy Richman
The genetics of hydatidiform moles: new lights on an ancient disease
Rima Slim, Amira Mehio
Developmental Programming of Hypothalamic Feeding Circuits
Sebastien Bouret, Richard B. Simerly
Human embryo and early fetus research
Harry Ostrer, D Wilson, N Hanley
Craniofacial malformations: intrinsic versus extrinsic neural crest cell defects in Treacher Collins and 22q11 deletion syndromes
Macie Walker, Paul Trainor
New development insights from high-throughput biological analysis in C. elegans
Jean-Claude Labbe, Richard Roy
Vesicoureteric reflux and renal malformations: a developmental problem
Murawski I.J., Indra R. Gupta
TopSocial and Behavioural Research February 2008
Predictors of psychological distress among individuals with a strong family history of malignant melanoma
Nadine Kasparian , Bettina Meiser , Phyllis Butow, Judy Simpson, Graham Mann
Cultural enhancement of a clinical service to meet the needs of indigenous people; genetic service development in response to issues for New Zealand Maori
RV Port, J Arnold, D Kerr, N Gravish, Ingrid Winship
Colorectal Cancer Survivors Undergoing Genetic Testing for Hereditary Non-Polyposis Colorectal Cancer (HNPCC): Motivational Factors and Psychosocial Functioning
Mary Jane Esplen , Lisa Madlensky, Melyssa Aronson, Heidi Rothenmund, Steve Gallinger, Kate Butler , Brenda Toner, Jiahui Wong, Mike Manno, John McLaughlin
A COMPARISON OF COUNSELEE AND COUNSELOR SATISFACTION IN REPRODUCTIVE GENETIC COUNSELING
C M Aalfs, F Oort, J de Haes, N Leschot, E Smets
Genetic testing for heart disease susceptibility: potential impact on motivation to quit smoking
Saskia Sanderson, Susan Michie
Young people's experiences of growing up in a family affected by Huntington's disease
K Forrest Keenan, Z Miedzybrodzka, E Van Teijlingen, L McKee, S A Simpson
Family system characteristics and psychological adjustment to cancer susceptibility genetic testing: a prospective study
I van Oostrom, H Meijers-Heijboer, H J Duivenvoorden, A H J T Brocker-Vriends, C J van Asperen, R H Sijmons, C Seynaeve, A R Van Gool, J G M Klijn, A Tibben
The Personal experience of Juvenile Huntingtons Disease: an interpretative phenomenological analysis of parents accounts of the primary features of a rare genetic condition
Jonathan A. Smith, Helen M. Brewer, Virginia Eatough, Cath A. Stanley, Neil W. Glendinning, Oliver W. J. Quarrell
Views of female breast cancer patients who donated biologic samples regarding storage and use of samples for genetic research
Kimberly A. Kaphingst, Jamie M. Janoff, Lyndsay N. Harris, Karen M. Emmons
