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Clinical Genetics|January 1, 1991
Glyceryl ethers in peroxisomal diseaseA Poulos, A Bankier, K Beckman, et al.Clinical Genetics|November 15, 2006
Spastin gene mutations in Bulgarian patients with hereditary spastic paraplegiaN Ivanova, A Löfgren, I Tournev, et al.Clinical Genetics|February 1, 1991
Using the polymerase chain reaction to maintain DNA probe inventories in clinical and diagnostic laboratoriesJ Tarleton, C E SchwartzClinical Genetics|May 23, 2006
Craniofacial malformations: intrinsic vs extrinsic neural crest cell defects in Treacher Collins and 22q11 deletion syndromesM B Walker, P A TrainorClinical Genetics|March 1, 1978
Detection of Fabry's disease heterozygotes by hair root analysisA L Beaudet, C T CaskeyClinical Genetics|May 29, 2010
C2orf37 mutational spectrum in Woodhouse-Sakati syndrome patientsA M Alazami, S A Schneider, D Bonneau, et al.Clinical Genetics|May 29, 2010
The utility of quantitative methylation assays at imprinted genes for the diagnosis of fetal and placental disordersD K Bourque, M S Peñaherrera, R K C Yuen, et al.Clinical Genetics|May 26, 2010
Favorably skewed X-inactivation accounts for neurological sparing in female carriers of Menkes diseaseV Desai, A Donsante, K J Swoboda, et al.Clinical Genetics|May 26, 2010
A large cohort study of GJB2 mutations in Japanese hearing loss patientsK Tsukada, S Nishio, S Usami, et al.Clinical Genetics|May 26, 2010
Developmental perspectives on copy number abnormalities of the 22q11.2 regionT Y Tan, C T Gordon, D J Amor, et al.Pageof 718