Showing results (1181-1190 of 5,631) with videos related to

Sort By:
Pageof 564
European Journal of Human Genetics : EJHG|January 9, 2014
Incidence of sickle cell disease in an unselected cohort of neonates born in Berlin, GermanyStephan Lobitz, Claudia Frömmel, Annemarie Brose, et al.
European Journal of Human Genetics : EJHG|October 4, 2012
Vascular and connective tissue anomalies associated with X-linked periventricular heterotopia due to mutations in Filamin AEyal Reinstein, Sophia Frentz, Tim Morgan, et al.
European Journal of Human Genetics : EJHG|October 4, 2012
Genome-wide linkage analysis is a powerful prenatal diagnostic tool in families with unknown genetic defectsMaria Arélin, Bernt Schulze, Bertram Müller-Myhsok, et al.
European Journal of Human Genetics : EJHG|May 1, 1997
CFTR gene mutations in adults with disseminated bronchiectasisE Girodon, C Cazeneuve, F Lebargy, et al.
European Journal of Human Genetics : EJHG|May 1, 1997
A YAC contig spanning the blepharophimosis-ptosis-epicanthus inversus syndrome and propionic acidemia lociM R Piemontese, E Memeo, M Carella, et al.
European Journal of Human Genetics : EJHG|August 11, 2022
Genetics follow up after rapid genomic sequencing in intensive care: current practices and recommendations for service deliveryFiona Lynch, Amy Nisselle, Zornitza Stark, et al.
European Journal of Human Genetics : EJHG|August 11, 2022
Identification of novel genes whose expression in adipose tissue affects body fat mass and distribution: an RNA-Seq and Mendelian Randomization studyStefan Konigorski, Jürgen Janke, Giannino Patone, et al.
European Journal of Human Genetics : EJHG|November 9, 2022
Is there a "pandemic effect" on individuals' willingness to take genetic tests?Thibaud Deruelle, Veronika Kalouguina, Philipp Trein, et al.
European Journal of Human Genetics : EJHG|August 15, 2022
KBG syndrome: videoconferencing and use of artificial intelligence driven facial phenotyping in 25 new patientsLily Guo, Jiyeon Park, Edward Yi, et al.
European Journal of Human Genetics : EJHG|November 8, 2022
Short stature in PRMT7 Mutations: first evidence of response to growth hormone treatmentGiulia Rodari, Roberta Villa, Matteo Porro, et al.
Pageof 564