Showing results (71-80 of 7,190) with videos related to
Sort By:
Pageof 719
Clinical Genetics|February 5, 2016
Molecular genetic analysis in 14 Czech Kabuki syndrome patients is confirming the utility of phenotypic scoringJ Paděrová, A Holubová, M Simandlová, et al.Clinical Genetics|February 1, 1989
Autosomal dominant lamellar ichthyosis exhibits an abnormal scale lipid patternB Melnik, W Küster, J Hollmann, et al.Clinical Genetics|February 1, 1989
Phenotype variability in the Miller acrofacial dysostosis syndrome. Report of two further patientsK H Chrzanowska, J P Fryns, M Krajewska-Walasek, et al.Clinical Genetics|June 2, 2016
Expanding the clinical picture of the MECP2 Duplication syndromeZ Lim, J Downs, K Wong, et al.Clinical Genetics|June 4, 2016
The homozygous R504C mutation in MTO1 gene is responsible for ONCE syndromeM Á Martín, M T García-Silva, G Barcia, et al.Clinical Genetics|April 11, 2016
Autosomal recessive IFT57 hypomorphic mutation cause ciliary transport defect in unclassified oral-facial-digital syndrome with short stature and brachymesophalangiaJ Thevenon, L Duplomb, S Phadke, et al.Clinical Genetics|April 12, 2016
National G6PD neonatal screening program in Gaza Strip of Palestine: rationale, challenges and recommendationsM M Sirdah, M S Al-Kahlout, N S ReadingClinical Genetics|November 1, 1989
Prospects for cancer control and prevention through geneticsJ J MulvihillClinical Genetics|November 1, 1989
Autosomal dominant polycystic kidney disease in the 1980'sO Z Dalgaard, S NørbyPageof 719