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1.
The c.1617del variant of TMEM260 is identified as the most frequent single gene determinant for Japanese patients with a specific type of congenital heart disease.
J Hum Genet;
69(5): 215-222, 2024 May.
Artículo
en Inglés
| MEDLINE | ID: mdl-38409496
2.
Functional characterization of variants found in Japanese patients with hereditary hemorrhagic telangiectasia.
Clin Genet;
105(5): 543-548, 2024 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-38225712
3.
Pregnancy and Delivery in Patients With Repaired Congenital Heart Diseaseã- A Retrospective Japanese Multicenter Study.
Circ J;
84(12): 2270-2274, 2020 11 25.
Artículo
en Inglés
| MEDLINE | ID: mdl-33055459
4.
Correction: The c.1617del variant of TMEM260 is identified as the most frequent single gene determinant for Japanese patients with a specific type of congenital heart disease.
J Hum Genet;
69(5): 223, 2024 May.
Artículo
en Inglés
| MEDLINE | ID: mdl-38459226
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