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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Dec 3, 2023. (Total: 223614Documents)
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Records 1 - 4 (of 4 Records)

Query Trace: Abnormalities and TBX1[original query]
TBX1 gene mutation screening in patients with non-syndromic Fallot tetralogy.
The Turkish journal of pediatrics 0 49 (1): 61-8.
Cabuk Feryal, Karabulut Halil G, Tuncali Timur, Karademir Selmin, Bozdayi Mithat, Tükün Ajl
Human gene copy number spectra analysis in congenital heart malformations.
Physiological genomics 2012 Feb .
Tomita-Mitchell A, Mahnke DK, Struble CA, Tuffnell ME, Stamm KD, Hidestrand M, Harris SE, Goetsch MA, Simpson PM, Bick DP, Broeckel U, Pelech AN, Tweddell JS, Mitchell ME
Genetic Imbalances in Argentinean Patients with Congenital Conotruncal Heart Defects.
Genes 2018 Sep 9 (9): .
Delea Marisol, Espeche Lucía D, Bruque Carlos D, Bidondo María Paz, Massara Lucía S, Oliveri Jaen, Brun Paloma, Cosentino Viviana R, Martinoli Celeste, Tolaba Norma, Picon Claudina, Ponce Zaldua María Eugenia, Ávila Silvia, Gutnisky Viviana, Perez Myriam, Furforo Lilian, Buzzalino Noemí D, Liascovich Rosa, Groisman Boris, Rittler Mónica, Rozental Sandra, Barbero Pablo, Dain Lilia
A novel TBX1 missense mutation in patients with syndromic congenital heart defects.
Biochemical and biophysical research communications 2018 3 499 (3): 563-569.
Jaouadi Amel, Tabebi Mouna, Abdelhedi Fatma, Abid Dorra, Kamoun Fatma, Chabchoub Imen, Maatoug Sirine, Doukali Hajer, Belghuith Neila, Ksentini Mohamed Ali, Keskes Leila Ammar, Triki Chahnez, Hachicha Mongia, Kamoun Samir, Kamoun Hass
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