Showing results (501-510 of 878) with videos related to

Sort By:
Pageof 88
Zentralblatt Fur Chirurgie|May 23, 2007
[Report on the workshop "workflow rectal cancer II" in Burghausen]R Bittner, J Burghardt, E Gross, et al.
American Journal of Medical Genetics. Part A|November 26, 2010
UBE2A deficiency syndrome: Mild to severe intellectual disability accompanied by seizures, absent speech, urogenital, and skin anomalies in male patientsNicole de Leeuw, Saskia Bulk, Andrew Green, et al.
American Journal of Human Genetics|July 11, 2006
Loss-of-function mutations in euchromatin histone methyl transferase 1 (EHMT1) cause the 9q34 subtelomeric deletion syndromeTjitske Kleefstra, Han G Brunner, Jeanne Amiel, et al.
Clinical Genetics|February 6, 2004
The clinical picture of the Börjeson-Forssman-Lehmann syndrome in males and heterozygous females with PHF6 mutationsG Turner, K M Lower, S M White, et al.
Critical Care Medicine|October 19, 2018
Long-Term Outcome of Patients With a Hematologic Malignancy and Multiple Organ Failure Admitted at the Intensive CareVera A de Vries, Marcella C A Müller, M Sesmu Arbous, et al.
Clinical Genetics|September 10, 2004
Genotype-phenotype studies in three families with mutations in the polyglutamine-binding protein 1 gene (PQBP1)T Kleefstra, C E Franken, Y H J M Arens, et al.
Genetics in Medicine Open|December 13, 2024
GenIDA, a participatory patient registry for genetic forms of intellectual disability provides detailed caregiver-reported information on 237 individuals with Koolen-de Vries syndromeFlorent Colin, Pauline Burger, Timothée Mazzucotelli, et al.
Critical Care Explorations|May 30, 2024
Development and Validation of a Prediction Model for 1-Year Mortality in Patients With a Hematologic Malignancy Admitted to the ICUJan-Willem H L Boldingh, M Sesmu Arbous, Bart J Biemond, et al.
Metabolism: Clinical and Experimental|December 3, 2014
Glucose-dependent leukocyte activation in patients with type 2 diabetes mellitus, familial combined hyperlipidemia and healthy controlsMarijke A de Vries, Arash Alipour, Boudewijn Klop, et al.
Nature Communications|November 6, 2024
Phenotypic and genetic characteristics of retinal vascular parameters and their association with diseasesSofía Ortín Vela, Michael J Beyeler, Olga Trofimova, et al.
Pageof 88