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1 Ergebnisse
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Screening Method for 22q11 Deletion Syndrome Involving the ..:
Felix-Julian Campos-Garcia
;
Addy-Manuela Castillo-Espinola
;
Carolina-Elizabeth Medina-Escobedo
...
Molecular Genetics. , 2022
Link:
https://doi.org/10.3390/cardiogenetics12030024
RT Journal T1
Screening Method for 22q11 Deletion Syndrome Involving the Use of TaqMan qPCR for TBX1 in Patients with Conotruncal Congenital Heart Disease
UL https://suche.suub.uni-bremen.de/peid=base-ftmdpi:oai:mdpi.com:_2035-8148_12_3_24_&Exemplar=1&LAN=DE A1 Felix-Julian Campos-Garcia A1 Addy-Manuela Castillo-Espinola A1 Carolina-Elizabeth Medina-Escobedo A1 Juan C. Zenteno A1 Julio-Cesar Lara-Riegos A1 Hector Rubio-Zapata A1 David Cruz-Robles A1 Ana-Isabel Velazquez-Ibarra PB Multidisciplinary Digital Publishing Institute YR 2022 K1 newborn screening congenital heart disease K1 22q11.2 syndrome K1 TBX1 JF Molecular Genetics LK http://dx.doi.org/https://doi.org/10.3390/cardiogenetics12030024 DO https://doi.org/10.3390/cardiogenetics12030024 SF ELIB - SuUB Bremen
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