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Clinical Genetics|May 1, 1978
Congenital hydrocephalus and cerebellar agenesisV M Riccardi, E S MarcusClinical Genetics|July 1, 1980
Binary developmental commitments in normal and abnormal human morphogenesisJ M FriedmanClinical Genetics|July 1, 1980
Prader-Willi syndrome and a bisatellited derivative of chromosome 15L P Wisniewski, M E Witt, F Ginsberg-Fellner, et al.Clinical Genetics|July 1, 1980
Clinical, hematological and genetic features of sickle-cell anemia and sickle cell-beta thalassemia in a Brazilian populationM A Zago, F F Costa, T C Freitas, et al.Clinical Genetics|May 1, 1984
Interstitial deletion of band q12 of chromosome 5G Dudin, D Alexander, F Talj, et al.Clinical Genetics|July 1, 1984
Linkage of plasma alpha-L-fucosidase (FUCA2) and the plasminogen (PLG) systemH Eiberg, J Mohr, L S NielsenClinical Genetics|July 1, 1985
Genetic linkage analysis of epidermolysis bullosa dystrophica, Cockayne-Touraine typeJ C Mulley, T Turner, C Nicholls, et al.Clinical Genetics|July 1, 1985
Autosomal dominant cataract and microcornea associated with myopia in a Sicilian familyF Mollica, S Li Volti, S Tomarchio, et al.Clinical Genetics|April 29, 2015
Evaluating a counselling strategy for diagnostic WES in paediatric neurology: an exploration of parents' information and communication needsL Krabbenborg, J Schieving, T Kleefstra, et al.Clinical Genetics|April 30, 2015
Prevalence of founder mutations in the BRCA1 and BRCA2 genes among unaffected women from the BahamasM Trottier, J Lunn, R Butler, et al.Pageof 719