Zespół SCID (Polish Wikipedia)

Analysis of information sources in references of the Wikipedia article "Zespół SCID" in Polish language version.

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Barbara Corneo, Despina Moshous, Tayfun Güngör, Nicolas Wulffraat, Pierre Philippet, Françoise Le Deist, Alain Fischer, Jean-Pierre de Villartay. Identical mutations in RAG1 or RAG2 genes leading to defective V(D)J recombinase activity can cause either T-B–severe combined immune deficiency or Omenn syndrome (Patients, materials, and methods: Patients). „Blood”. 97 (9), s. 2772–2776, 1 maja 2001. American Society of Hematology. DOI: 10.1182/blood.V97.9.2772. ISSN 0006-4971. OCLC 01536582. (ang.).
Capucine Picard, H. Bobby Gaspar, Waleed Al-Herz, Aziz Bousfiha i inni. International Union of Immunological Societies: 2017 Primary Immunodeficiency Diseases Committee Report on Inborn Errors of Immunity. „Journal of Clinical Immunology”. 38 (1), s. 96–128, 2017. DOI: 10.1007/s10875-017-0464-9. ISSN 0271-9142. (ang.).

Gene Therapy and Gene Editing. W: Mike Berridge: The Edge of Life: Controversies and Challenges in Human Health. T. 33. Bridget Williams Books, 2015, s. 48. ISBN 978-0-908321-34-6. [dostęp 2016-05-14].

Clyde Haberman: ‘The Boy in the Bubble’ Moved a World He Couldn’t Touch. The New York Times, 6 grudnia 2015. [dostęp 2016-05-14]. [zarchiwizowane z tego adresu (2015-12-07)]. (ang.).

Severe combined immunodeficiency | Disease | Your Questions Answered | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program. rarediseases.info.nih.gov, 27 maja 2014. [dostęp 2016-05-14]. [zarchiwizowane z tego adresu (18 września 2015)]. (ang.).
Clyde Haberman: ‘The Boy in the Bubble’ Moved a World He Couldn’t Touch. The New York Times, 6 grudnia 2015. [dostęp 2016-05-14]. [zarchiwizowane z tego adresu (2015-12-07)]. (ang.).

Barbara Corneo, Despina Moshous, Tayfun Güngör, Nicolas Wulffraat, Pierre Philippet, Françoise Le Deist, Alain Fischer, Jean-Pierre de Villartay. Identical mutations in RAG1 or RAG2 genes leading to defective V(D)J recombinase activity can cause either T-B–severe combined immune deficiency or Omenn syndrome (Patients, materials, and methods: Patients). „Blood”. 97 (9), s. 2772–2776, 1 maja 2001. American Society of Hematology. DOI: 10.1182/blood.V97.9.2772. ISSN 0006-4971. OCLC 01536582. (ang.).
Capucine Picard, H. Bobby Gaspar, Waleed Al-Herz, Aziz Bousfiha i inni. International Union of Immunological Societies: 2017 Primary Immunodeficiency Diseases Committee Report on Inborn Errors of Immunity. „Journal of Clinical Immunology”. 38 (1), s. 96–128, 2017. DOI: 10.1007/s10875-017-0464-9. ISSN 0271-9142. (ang.).