Σύνδρομο Γιάκομπσεν (Greek Wikipedia)

Analysis of information sources in references of the Wikipedia article "Σύνδρομο Γιάκομπσεν" in Greek language version.

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Grossfeld, Paul D.; Mattina, Teresa; Lai, Zona; Favier, Remi; Jones, Ken Lyons; Cotter, Finbarr; Jones, Christopher (2004-08-15). «The 11q terminal deletion disorder: a prospective study of 110 cases». American Journal of Medical Genetics. Part A 129A (1): 51–61. doi:10.1002/ajmg.a.30090. ISSN 1552-4825. PMID 15266616. https://pubmed.ncbi.nlm.nih.gov/15266616/.
Φαβιέρ, Ρεμί; Ακσούμοφ, Νατάσα; Μάτσον, Σάρα; Γκρόσφιλντ, Πολ (1 Σεπτεμβρίου 2015). «Jacobsen syndrome: Advances in our knowledge of phenotype and genotype» (στα αγγλικά). American Journal of Medical Genetics Part C: Seminars in Medical Genetics 169 (3): 239–250. doi:10.1002/ajmg.c.31448. PMID 26285164.
Favier, Remi; Akshoomoff, Natacha; Mattson, Sarah; Grossfeld, Paul (2015). «Jacobsen syndrome: Advances in our knowledge of phenotype and genotype» (στα αγγλικά). American Journal of Medical Genetics Part C: Seminars in Medical Genetics 169 (3): 239–250. doi:10.1002/ajmg.c.31448. ISSN 1552-4876. https://onlinelibrary.wiley.com/doi/abs/10.1002/ajmg.c.31448.

«Jacobsen syndrome: MedlinePlus Genetics». medlineplus.gov (στα Αγγλικά). Ανακτήθηκε στις 15 Ιουλίου 2021.

Grossfeld, Paul D.; Mattina, Teresa; Lai, Zona; Favier, Remi; Jones, Ken Lyons; Cotter, Finbarr; Jones, Christopher (2004-08-15). «The 11q terminal deletion disorder: a prospective study of 110 cases». American Journal of Medical Genetics. Part A 129A (1): 51–61. doi:10.1002/ajmg.a.30090. ISSN 1552-4825. PMID 15266616. https://pubmed.ncbi.nlm.nih.gov/15266616/.
Φαβιέρ, Ρεμί; Ακσούμοφ, Νατάσα; Μάτσον, Σάρα; Γκρόσφιλντ, Πολ (1 Σεπτεμβρίου 2015). «Jacobsen syndrome: Advances in our knowledge of phenotype and genotype» (στα αγγλικά). American Journal of Medical Genetics Part C: Seminars in Medical Genetics 169 (3): 239–250. doi:10.1002/ajmg.c.31448. PMID 26285164.

Reference, Genetics Home. «Jacobsensyndrome». Genetics Home Reference (στα Αγγλικά).

Grossfeld, Paul D.; Mattina, Teresa; Lai, Zona; Favier, Remi; Jones, Ken Lyons; Cotter, Finbarr; Jones, Christopher (2004-08-15). «The 11q terminal deletion disorder: a prospective study of 110 cases». American Journal of Medical Genetics. Part A 129A (1): 51–61. doi:10.1002/ajmg.a.30090. ISSN 1552-4825. PMID 15266616. https://pubmed.ncbi.nlm.nih.gov/15266616/.

«Orphanet: Jacobsen syndrome». www.orpha.net (στα Αγγλικά). Ανακτήθηκε στις 15 Ιουλίου 2021.

Favier, Remi; Akshoomoff, Natacha; Mattson, Sarah; Grossfeld, Paul (2015). «Jacobsen syndrome: Advances in our knowledge of phenotype and genotype» (στα αγγλικά). American Journal of Medical Genetics Part C: Seminars in Medical Genetics 169 (3): 239–250. doi:10.1002/ajmg.c.31448. ISSN 1552-4876. https://onlinelibrary.wiley.com/doi/abs/10.1002/ajmg.c.31448.

Grossfeld, Paul D.; Mattina, Teresa; Lai, Zona; Favier, Remi; Jones, Ken Lyons; Cotter, Finbarr; Jones, Christopher (2004-08-15). «The 11q terminal deletion disorder: a prospective study of 110 cases». American Journal of Medical Genetics. Part A 129A (1): 51–61. doi:10.1002/ajmg.a.30090. ISSN 1552-4825. PMID 15266616. https://pubmed.ncbi.nlm.nih.gov/15266616/.
Favier, Remi; Akshoomoff, Natacha; Mattson, Sarah; Grossfeld, Paul (2015). «Jacobsen syndrome: Advances in our knowledge of phenotype and genotype» (στα αγγλικά). American Journal of Medical Genetics Part C: Seminars in Medical Genetics 169 (3): 239–250. doi:10.1002/ajmg.c.31448. ISSN 1552-4876. https://onlinelibrary.wiley.com/doi/abs/10.1002/ajmg.c.31448.