Results 131 to 140 of about 1,575 (156)
Some of the next articles are maybe not open access.
Impaired instrumental learning in Spred1−/− mice, a model for a rare RASopathy
Genes, Brain and Behavior, 2021Akihiko Yoshimura +2 more
exaly
Microarray and RASopathy‐disorder testing in fetuses with increased nuchal translucency
Ultrasound in Obstetrics and Gynecology, 2020Pierre Sinajon, Syed Wasim
exaly
[RASopathies and hematologic abnormalities].
[Rinsho ketsueki] The Japanese journal of clinical hematology, 2016Whole exome sequencing with a next generation sequencer is increasingly being used for identifying new genes and for diagnosing genetic disorders. Numerous causative genes have been identified in Mendelian disorders as well as cancers and multifactorial disorders. Among inborn errors of development, recent advances have been noted in the identification
openaire +1 more source
ClinGen’s RASopathy Expert Panel consensus methods for variant interpretation
Genetics in Medicine, 2018Mitchell W Dillon +2 more
exaly
Systemic lupus erythematosus associated with RASopathy
Modern Rheumatology Case Reports, 2017Hisashi Yamanaka +2 more
exaly
Emerging Hypotheses on the Pathogenesis of Rasopathy-Associated Cardiomyopathies
Nihon Shoni Junkanki Gakkai Zasshi = Pediatric Cardiology and Cardiac Surgery, 2023exaly
Juvenile myelomonocytic leukemia – A bona fide RASopathy syndrome
Best Practice and Research in Clinical Haematology, 2020Mrinal Patnaik, Terra Lasho
exaly
NRAS associated RASopathy and embryonal rhabdomyosarcoma
American Journal of Medical Genetics, Part A, 2020Jacob Hogue
exaly