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Clinical Genetics|March 1, 1990
High resolution banding of an unusual reciprocal translocation in recurrent abortionsP M Kroisel, W Rosenkranz
Clinical Genetics|December 15, 2012
Myoclonus-dystonia and Silver-Russell syndrome resulting from maternal uniparental disomy of chromosome 7M B Sheridan, A Bytyci Telegrafi, V Stinnett, et al.
Clinical Genetics|December 18, 2012
PTEN mosaicism with features of Cowden syndromeA Gammon, K Jasperson, R Pilarski, et al.
Clinical Genetics|December 4, 2012
New evidence for, and challenges in, linking small CGG repeat expansion FMR1 alleles with Parkinson's diseaseD Z Loesch, F Tassone, J Lo, et al.
Clinical Genetics|September 13, 2013
The impact of next generation sequencing on the analysis of breast cancer susceptibility: a role for extremely rare genetic variation?F S M Hilbers, M P G Vreeswijk, C J van Asperen, et al.
Clinical Genetics|September 17, 2013
A systematic approach to assessing the clinical significance of genetic variantsH Duzkale, J Shen, H McLaughlin, et al.
Clinical Genetics|August 20, 2013
The future in clinical genetics: affective forecasting biases in patient and clinician decision makingS A Peters, S M Laham, N Pachter, et al.
Clinical Genetics|August 29, 2013
Intrafamilial phenotypic variability in four families with Anderson-Fabry diseaseM Rigoldi, D Concolino, A Morrone, et al.
Clinical Genetics|September 3, 2013
Broadening the phenotype of LRP2 mutations: a new mutation in LRP2 causes a predominantly ocular phenotype suggestive of Stickler syndromeI Schrauwen, M Sommen, C Claes, et al.
Clinical Genetics|September 3, 2013
Overexpression of G100S mutation in PRKAG2 causes Wolff-Parkinson-White syndrome in zebrafishB L Zhang, Z Ye, R L Xu, et al.
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