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Clinical Genetics|May 8, 2010
Stüve-Wiedemann syndrome: long-term follow-up and genetic heterogeneityC Jung, N Dagoneau, G Baujat, et al.
Clinical Genetics|May 8, 2010
Genetics professionals' experiences with grief and loss: implications for support and trainingG Geller, C H Rushton, C Francomano, et al.
Clinical Genetics|May 12, 2010
Mutational spectrum in the cardiac transcription factor gene NKX2.5 (CSX) associated with congenital heart diseaseB Stallmeyer, H Fenge, U Nowak-Göttl, et al.
Clinical Genetics|April 24, 2010
The human phenotype ontologyP N Robinson, S Mundlos
Clinical Genetics|April 24, 2010
Clinical evaluation of DFN3 patients with deletions in the POU3F4 locus and detection of carrier female using MLPAM H Song, H K Lee, J Y Choi, et al.
Clinical Genetics|April 24, 2010
Mandibulofacial dysostosis, microtia, and limb anomalies in a newborn: a new form of acrofacial dysostosis syndrome?Y Zhang, Y Dai, Y Liu, et al.
Clinical Genetics|August 8, 2009
Review of the Lynch syndrome: history, molecular genetics, screening, differential diagnosis, and medicolegal ramificationsH T Lynch, P M Lynch, S J Lanspa, et al.
Clinical Genetics|August 8, 2009
Neuromuscular features in Marfan syndromeN c Voermans, J Timmermans, N van Alfen, et al.
Clinical Genetics|August 8, 2009
A child cohort study from southern Italy enlarges the genetic spectrum of hypertrophic cardiomyopathyG Frisso, G Limongelli, G Pacileo, et al.
Clinical Genetics|April 8, 2010
High frequency of ETFDH c.250G>A mutation in Taiwanese patients with late-onset lipid storage myopathyM-Y Lan, M-H Fu, Y-F Liu, et al.
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