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Clinical Genetics|March 17, 2017
Reassessing the clinical spectrum associated with hereditary leiomyomatosis and renal cell carcinoma syndrome in French FH mutation carriersM Muller, S Ferlicot, M Guillaud-Bataille, et al.
Clinical Genetics|April 4, 2017
Genetics of hypertrophic cardiomyopathy: A review of current stateM Sabater-Molina, I Pérez-Sánchez, J P Hernández Del Rincón, et al.
Clinical Genetics|April 4, 2017
Study of the Huntington's disease IT-15 gene in different ethnic groups in EcuadorC Paz-Y-Miño, C Salazar-Ruales, J M García-Cárdenas, et al.
Clinical Genetics|April 4, 2017
New EPCAM founder deletion in Polish populationD Dymerska, K Gołębiewska, M Kuświk, et al.
Clinical Genetics|April 4, 2017
Genome-wide linkage and sequence analysis challenge CCDC66 as a human retinal dystrophy candidate gene and support a distinct NMNAT1-related fundus phenotypeA O Khan, B S Budde, P Nürnberg, et al.
Clinical Genetics|April 9, 2017
PGAP3-related hyperphosphatasia with mental retardation syndrome: Report of 10 new patients and a homozygous founder mutationM S Abdel-Hamid, M Y Issa, G A Otaify, et al.
Clinical Genetics|February 25, 2017
A novel DNAJB6 mutation causes dominantly inherited distal-onset myopathy and compromises DNAJB6 functionP-C Tsai, Y-S Tsai, B-W Soong, et al.
Clinical Genetics|March 15, 2019
Assessing optimism and pessimism about genomic medicine: Development of a genomic orientation scaleCaroline Horrow, Joel E Pacyna, Erica J Sutton, et al.
Clinical Genetics|February 22, 2019
Systematic review of quality of life in persons with hereditary thoracic aortic aneurysm and dissection diagnosesGry Velvin, Jan E Wilhelmsen, Heidi Johansen, et al.
Clinical Genetics|February 1, 1986
Sanfilippo disease in GreeceN G Beratis, S L Sklower, L Wilbur, et al.
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