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Journal of Human Genetics|September 1, 2017
Santos syndrome is caused by mutation in the WNT7A geneLeandro U Alves, Silvana Santos, Camila M Musso, et al.American Journal of Medical Genetics|April 1, 1984
Tandem dup (1p) within the short arm of chromosome 1 in a child with ambiguous genitalia and multiple congenital anomaliesB R Elejalde, J M Opitz, M M de Elejalde, et al.European Journal of Human Genetics : EJHG|January 17, 2003
PTPN11 mutations are not responsible for the Cardiofaciocutaneous (CFC) syndromeM I Kavamura, M G Pomponi, M Zollino, et al.American Journal of Medical Genetics|April 1, 1984
Syndrome of multiple pterygia, camptodactyly, facial anomalies, hypoplastic lungs and heart, cystic hygroma, and skeletal anomalies: delineation of a new entity and review of lethal forms of multiple pterygium syndromeH Chen, L Immken, R Lachman, et al.Nature Communications|June 3, 2020
Suppression of unwanted CRISPR-Cas9 editing by co-administration of catalytically inactivating truncated guide RNAsJohn C Rose, Nicholas A Popp, Christopher D Richardson, et al.Cell Chemical Biology|September 8, 2023
Profiling of drug resistance in Src kinase at scale uncovers a regulatory network coupling autoinhibition and catalytic domain dynamicsSujata Chakraborty, Ethan Ahler, Jessica J Simon, et al.Journal of Applied Microbiology|February 19, 2002
Salmonella enterica serotype Enteritidis phage types 4, 7, 6, 8, 13a, 29 and 34: a comparative analysis of genomic fingerprints from geographically distant isolatesErnesto Liebana, L Garcia-Migura, J Guard-Petter, et al.International Clinical Psychopharmacology|June 28, 2000
Increased psychological responses and divergent neuroendocrine responses to m-CPP and ipsapirone in patients with panic disorderA Broocks, B Bandelow, A George, et al.Cardiovascular and Interventional Radiology|December 28, 2025
Effectiveness and Safety of Image-Guided Renal Biopsies: Insights from 5,235 Procedures in the German Society for Interventional Radiology and Minimally Invasive Therapy (DeGIR) RegistryR Ocker-Serger, M Opitz, L Klüner, et al.Clinical Genetics|May 11, 1975
Familial Kallmann syndrome with unilateral renal aplasiaJ D Wegenke, D T Uehling, J B Wear, et al.Pageof 34