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Xq25 duplication: the crucial role of the STAG2 gene in this novel human cohesinopathy.
- Published in:
- Clinical Genetics, 2016, v. 89, n. 1, p. 68, doi. 10.1111/cge.12567
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- Article
Molecular findings and clinical data in a cohort of 150 patients with anophthalmia/microphthalmia.
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- Clinical Genetics, 2014, v. 86, n. 4, p. 326, doi. 10.1111/cge.12275
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- Article
Gorlin syndrome presenting as prenatal chylothorax in a girl.
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- Prenatal Diagnosis, 2005, v. 25, n. 11, p. 997, doi. 10.1002/pd.1231
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- Article
努南综合征的皮肤病表现.
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- British Journal of Dermatology, 2019, v. 180, n. 6, p. e266, doi. 10.1111/bjd.17978
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- Article
Dermatological manifestations in Noonan syndrome.
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- British Journal of Dermatology, 2019, v. 180, n. 6, p. e249, doi. 10.1111/bjd.17961
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- Article
Dermatological manifestations in Noonan syndrome: a prospective multicentric study of 129 patients positive for mutation.
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- British Journal of Dermatology, 2019, v. 180, n. 6, p. 1438, doi. 10.1111/bjd.17404
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- Article
心脸皮肤综合症中的皮肤表现.
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- British Journal of Dermatology, 2019, v. 180, n. 1, p. e30, doi. 10.1111/bjd.17385
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- Article
Dermatological manifestations in cardiofaciocutaneous syndrome.
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- British Journal of Dermatology, 2019, v. 180, n. 1, p. e17, doi. 10.1111/bjd.17371
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- Article
Dermatological manifestations in cardiofaciocutaneous syndrome: a prospective multicentric study of 45 mutation‐positive patients.
- Published in:
- British Journal of Dermatology, 2019, v. 180, n. 1, p. 172, doi. 10.1111/bjd.17077
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- Article