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Clinical Genetics|March 1, 1977
The distribution of ancestral secondary cases in Parkinson's diseaseW I Young, W E Martin, V E AndersonClinical Genetics|March 1, 1977
Dermatoglyphics in Cri du Chat syndromeH Shiono, J I Kadowaki, H KazamaClinical Genetics|June 1, 1993
Direct molecular diagnosis of myotonic dystrophyB K Hecht, A Donnelly, A K Gedeon, et al.Clinical Genetics|June 1, 1993
Intrafamilial variability in the clinical expression of familial hypercholesterolemia: importance of risk factor determination for genetic counsellingM J Kotze, H J Davis, S Bissbort, et al.Clinical Genetics|June 1, 1993
Inheritance of intrahepatic cholestasis of pregnancy in one kindredM L Hirvioja, S KivinenClinical Genetics|January 1, 1993
Infant mortality in myotonic dystrophy in Saguenay-Lac-St-Jean: a historical perspectiveT N Dao, J Mathieu, J P Bouchard, et al.Clinical Genetics|January 1, 1993
A balanced autosomal translocation (3;9) associated with primary hypogonadism and dorsal spine stenosisP J Hughes, J M Edwards, M A Ridler, et al.Clinical Genetics|February 1, 1993
Attitudes of Dutch general practitioners towards presymptomatic DNA-testing for Huntington diseaseR Thomassen, A Tibben, M F Niermeijer, et al.Clinical Genetics|February 1, 1993
Acute adrenal crisis complicating hypertensive congenital adrenal hyperplasia due to 11 beta-hydroxylase deficiencyY LielPageof 718