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Mastocytosis in a Case of Noonan Syndrome Caused by a De Novo Pathogenic CBL Variant.
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- Yonago Acta Medica, 2023, v. 66, n. 4, p. 463, doi. 10.33160/yam.2023.11.005
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- Article
Recurrent Erythema Nodosum in a Child with a SHOC2 Gene Mutation.
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- Yonago Acta Medica, 2019, v. 62, n. 1, p. 159, doi. 10.33160/yam.2019.03.022
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- Article
Apoptotic Cell Death in Human Gastric Carcinoma: Analysis by Terminal Deoxynucleotidyl Transferase-mediated dUTP-biotin Nick End Labeling.
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- Cancer Science, 1994, v. 85, n. 9, p. 939, doi. 10.1111/j.1349-7006.1994.tb02972.x
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- Article
Apoptosis occurs more frequently in metastatic foci than in primary lesions of human colorectal carcinomas: Analysis by terminal-deoxynucleotidyl-transferase-mediated dUTP-biotin nick end labeling.
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- International Journal of Cancer, 1996, v. 65, n. 2, p. 173, doi. 10.1002/(SICI)1097-0215(19960117)65:2<173::AID-IJC8>3.0.CO;2-W
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- Article
Clinical course of a Japanese patient with developmental delay linked to a small 6q16.1 deletion.
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- Human Genome Variation, 2022, v. 9, n. 1, p. 1, doi. 10.1038/s41439-022-00194-w
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- Article
Duchenne muscular dystrophy–like phenotype in an LGMD2I patient with novel FKRP gene variants.
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- Human Genome Variation, 2020, v. 7, n. 1, p. 1, doi. 10.1038/s41439-020-0099-x
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- Article