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Journal of Medical Case Reports|May 15, 2016
Insulin-like growth factor type 1 deficiency in a Moroccan patient with de novo inverted duplication 9p24p12 and developmental delay: a case reportSaadia Amasdl, Abdelhafid Natiq, Siham Chafai Elalaoui, et al.
Chromosoma|November 24, 2023
Karyotypes of water frogs from the Pelophylax esculentus complex: results of cross-species chromosomal paintingDmitrij Dedukh, Antonina Maslova, Ahmed Al-Rikabi, et al.
Nursing & Health Sciences|February 27, 2003
Lessons learned as a research assistant studying ambulatory blood pressure in elderly Japanese stroke patientsChie Nishimura, Ryutaro Takahashi, Shigeko Miyamoto, et al.
European Journal of Human Genetics : EJHG|July 26, 2000
An essential SMN interacting protein (SIP1) is not involved in the phenotypic variability of spinal muscular atrophy (SMA)C Helmken, A Wetter, S Rudnik-Schöneborn, et al.
Biomedizinische Technik. Biomedical Engineering|October 13, 2011
Bioelectric and biomagnetic measurements are differentially sensitive to spiral currentsJens Haueisen, Alexander Dietzel, Mario Liehr, et al.
American Journal of Medical Genetics. Part A|December 8, 2005
Overrepresentation of small supernumerary marker chromosomes (sSMC) from chromosome 6 origin in cases with multiple sSMCThomas Liehr, Heike Starke, Gabriele Senger, et al.
Methods in Molecular Biology (Clifton, N.J.)|September 21, 2014
New BAC probe set to narrow down chromosomal breakpoints in small and large derivative chromosomes, especially suited for mosaic conditionsAhmed B Hamid, Xiaobo Fan, Nadezda Kosyakova, et al.
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