Results 141 to 150 of about 18,361 (285)

Clinical Utility of Multiplex Ligation-Dependent Probe Amplification in the Genetic Assessment of Patients with Myelodysplastic Syndrome. [PDF]

Biomedicines
Valeva R, Levkova M, Yahya D, Hachmeriyan M, Micheva I.   +4 more
europepmc   +1 more source

Intra and inter-species ANI values for the 44 <i>Aeromonas</i> genomes and identification on the basis of the MLPA and ANI (mislabeled genomes in bold).

, 2015
Roxana Beaz‐Hidalgo, J. Hossain Mohammad, Liles Mark R., Figueras Maria-Jose   +3 more
openalex   +2 more sources

Multiplex Ligation-Dependent Probe Amplification (MLPA) for Prenatal Diagnosis of Common Aneuploidies.

Methods in molecular biology, 2018
J. Schouten, P. van Vught, R. Galjaard
semanticscholar   +1 more source

Integrating molecular profiling into glioma diagnosis: implications of the WHO-CNS5-2021 classification of adult-type diffuse gliomas in Colombian patients. [PDF]

Front Neurol
Echeverría O, Patiño-Aldana AF, Chinchilla AM, Contreras N, Peralta S, Caballero N, Tovar HV, Palacio JM, Uribe V, Mineo-Pachón M, Velandia F, Castillo WMR, Valero N, Silgado-Guzmán DF, Ondo-Mendez A, Fonseca-Mendoza DJ.   +15 more
europepmc   +1 more source

MLPA as first screening method for the detection of microduplications and microdeletions in patients with X-linked mental retardation [PDF]

, 2007
Irene Madrigal, Laia Rodríguez‐Revenga, Célia Bádenas, Aurora Sánchez, Francisco Martı́nez, Isabel Fernández, Miguel Fernández‐Burriel, Montserrat Milà   +7 more
openalex   +1 more source

The Application of the NGS and MLPA Methods in the Molecular Diagnostics of Lynch Syndrome. [PDF]

Diagnostics (Basel)
Rako I, Vinceljak E, Popovic M, Zigman T.   +3 more
europepmc   +1 more source

Nonsendromik mental retardasyonlu hastaların subtelomerik MLPA ile incelenmesi

, 2021
93
openaire   +1 more source

Clinical application value of targeted amplicon sequencing technology in fetuses with uniparental disomy-related imprinting disorders: a multicenter study. [PDF]

J Transl Med
Liu N, Huang S, Zhang B, Zhou Y, Jin C, Sun P, Yang L, Wang X, Hu Y, Jin H, Wang B, Chen S, Yang X, Li J, Sun X, Liu W, Wei Y, Mu K, Liu L, Feng Y, Shi P, Kong X.   +21 more
europepmc   +1 more source

MLPA based detection of mutations in the dystrophin gene of 180 Polish families with Duchenne/Becker muscular dystrophy

, 2014
Janusz Zimowski, Diana Massalska, Mariola Holding, Sylwia Jadczak, E Fidziańska, Anna Łusakowska, Anna Kostera‐Pruszczyk, Anna Kamińska, Jacek Zaremba   +8 more
openalex   +2 more sources

IDENTIFICAÇÃO POR MLPA DIGITAL DE ALTERAÇÕES GENÉTICAS RELEVANTES EM PACIENTES IKZF1PLUS COM LLA-CPB

, 2022
CB Blunck, TC Barbosa, BA Lopes, CAP Poubel, MB Mansur, M Emerenciano   +5 more
openalex   +1 more source