Results 161 to 170 of about 62,351 (250)

Delineation of a de novo 7q21.3q31.1 Deletion by CGH-SNP Arrays in a Girl with Multiple Congenital Anomalies Including Severe Glaucoma [PDF]

, 2013
Lizeth Martínez‐Jacobo, Carlos Córdova‐Fletes, Rocío Ortiz‐López, Fernando Silva, C. Saucedo-Carrasco, Augusto Rojas-Martı́nez   +5 more
openalex   +1 more source

Workflow Analysis for CGH Generation with Speckle Reduction and Occlusion Culling Using GPU Acceleration. [PDF]

Sensors (Basel)
Serón FJ, Blesa A, Sanz D.
europepmc   +1 more source

Additional file 5: of Prematurity, ventricular septal defect and dysmorphisms are independent predictors of pathogenic copy number variants: a retrospective study on array-CGH results and phenotypical features of 293 children with neurodevelopmental disorders and/or multiple congenital anomalies

, 2018
Ilenia Maini, Ivan Ivanovski, Olivera Djurić, Stefano Giuseppe Caraffi, Edoardo Errichiello, Michela Marinelli, Federico Franchi, Veronica Bizzarri, Simonetta Rosato, Marzia Pollazzon, Chiara Gelmini, Michela Malacarne, Carlo Fusco, G Gargano, Sergio Bernasconi, Orsetta Zuffardi, Livia Garavelli   +16 more
openalex   +1 more source

Forging forward: SG60 and Changi General Hospital at 90. [PDF]

Singapore Med J
Ng KC, Siau C, Lee CE, Fock KM, Png GK, Yu JX.   +5 more
europepmc   +1 more source

A New Normalizing Algorithm for BAC CGH Arrays with Quality Control Metrics [PDF]

, 2011
Jeffrey C. Miecznikowski, Daniel P. Gaile, Song Liu, Lori Shepherd, Norma J. Nowak   +4 more
openalex   +1 more source

Array CGH demonstrates characteristic aberration signatures in human papillary thyroid carcinomas governed by RET/PTC [PDF]

, 2008
Kristian Unger, Eva Malisch, Gerry Thomas, Herbert Braselmann, Axel Walch, Gerhard Jackl, Paul D. Lewis, Edmund Lengfelder, Bogdanova Ti, Johannes Wienberg, Horst Zitzelsberger   +10 more
openalex   +1 more source

A Retrospective Study of Ultrasound-Guided C2 Transverse Process Injection with Myofascial Release for Cervicogenic Headache. [PDF]

J Pain Res
Hao L, Guo Y, Song L, Zhang L, Mi J.
europepmc   +1 more source

DETECTING COPY NUMBER VARIATIONS FROM ARRAY CGH DATA BASED ON A CONDITIONAL RANDOM FIELD MODEL

, 2010
Xiao-Lin Yin, Jing Li
openalex   +2 more sources

Partial Monosomy 21q Due to De Novo t(15;21)(q26.3;q22.11): A Case Report with Clinical and Molecular Findings. [PDF]

Appl Clin Genet
Nojehdeh ST, Fattahi T, Arish S, Mokabber H, Nobakht R, Davarnia S, Davarnia B.   +6 more
europepmc   +1 more source

Covering the Year in CGH: 2019 [PDF]

Clinical Gastroenterology and Hepatology, 2020
openaire   +2 more sources