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Clinical Genetics|August 1, 1981
Calf hypertrophy and asymmetry in female carriers of X-linked Duchenne muscular dystrophy: an over-diagnosed clinical manifestationN P Cavanagh, M A PreeceClinical Genetics|September 1, 1981
Histidinaemia in Sweden. Report on a neonatal screening programmeJ Alm, G Holmgren, A Larsson, et al.Clinical Genetics|May 15, 2015
X-chromosome inactivation in female patients with Fabry diseaseL Echevarria, K Benistan, A Toussaint, et al.Clinical Genetics|May 14, 2015
Regulator of dendritic cell migration, ASAP1 is associated with increased susceptibility to tuberculosisS WaltlClinical Genetics|June 1, 1983
Comparative diagnostic value of phenylalanine challenge and phenylalanine hydroxylase activity in phenylketonuriaM C Hsieh, H K Berry, M K Bofinger, et al.Clinical Genetics|May 1, 1983
Fetal mortality in oral cleft families: data from Indiana and MontrealK R Dronamraju, D BixlerClinical Genetics|May 1, 1983
Autosomal dominant inheritance of conductive deafness due to stapedial anomalies, external ear malformations and congenital facial palsyS Sellars, P BeightonClinical Genetics|August 1, 1978
In vitro studies of the interaction of calcium ions and other divalent cations with the Lp(a) lipoprotein and other isolated serum lipoproteinsG Dahlén, C Ericson, K BergClinical Genetics|August 1, 1978
Cluster of cystic fibrosis cases in a limited area of Brittany (France)E Bois, J Feingold, F Demenais, et al.Pageof 719