Σύνδρομο Μπάρμπερ-Σέι (Greek Wikipedia)

Analysis of information sources in references of the Wikipedia article "Σύνδρομο Μπάρμπερ-Σέι" in Greek language version.

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archive.org

«Human Dermo-1 has attributes similar to twist in early bone development». Bone 27 (5): 591–602. November 2000. doi:10.1016/S8756-3282(00)00380-X. PMID 11062344. https://archive.org/details/sim_bone_2000-11_27_5/page/591.

doi.org

dx.doi.org

«Recurrent Mutations in the Basic Domain of TWIST2 Cause Ablepharon Macrostomia and Barber-Say Syndromes». American Journal of Human Genetics 97 (1): 99–110. July 2015. doi:10.1016/j.ajhg.2015.05.017. PMID 26119818.
«TWIST family of basic helix-loop-helix transcription factors mediate human mesenchymal stem cell growth and commitment». Stem Cells 27 (10): 2457–68. October 2009. doi:10.1002/stem.181. PMID 19609939.
«Human Dermo-1 has attributes similar to twist in early bone development». Bone 27 (5): 591–602. November 2000. doi:10.1016/S8756-3282(00)00380-X. PMID 11062344. https://archive.org/details/sim_bone_2000-11_27_5/page/591.
«TWIST2 gene mutation». Clinical Case Reports 5 (7): 1167–1169. July 2017. doi:10.1002/ccr3.1014. PMID 28680619.

nih.gov

ncbi.nlm.nih.gov

«Recurrent Mutations in the Basic Domain of TWIST2 Cause Ablepharon Macrostomia and Barber-Say Syndromes». American Journal of Human Genetics 97 (1): 99–110. July 2015. doi:10.1016/j.ajhg.2015.05.017. PMID 26119818.
«TWIST family of basic helix-loop-helix transcription factors mediate human mesenchymal stem cell growth and commitment». Stem Cells 27 (10): 2457–68. October 2009. doi:10.1002/stem.181. PMID 19609939.
«Human Dermo-1 has attributes similar to twist in early bone development». Bone 27 (5): 591–602. November 2000. doi:10.1016/S8756-3282(00)00380-X. PMID 11062344. https://archive.org/details/sim_bone_2000-11_27_5/page/591.
«TWIST2 gene mutation». Clinical Case Reports 5 (7): 1167–1169. July 2017. doi:10.1002/ccr3.1014. PMID 28680619.

pubmedcentral.nih.gov

«Recurrent Mutations in the Basic Domain of TWIST2 Cause Ablepharon Macrostomia and Barber-Say Syndromes». American Journal of Human Genetics 97 (1): 99–110. July 2015. doi:10.1016/j.ajhg.2015.05.017. PMID 26119818.
«TWIST2 gene mutation». Clinical Case Reports 5 (7): 1167–1169. July 2017. doi:10.1002/ccr3.1014. PMID 28680619.

rarediseases.info.nih.gov

«Barber Say syndrome | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program». rarediseases.info.nih.gov. Ανακτήθηκε στις 21 Ιανουαρίου 2019.

omim.org

OMIM.Org: Barber-Say Syndrome

orpha.net

«Orphanet: Barber Say syndrome». www.orpha.net (στα Αγγλικά). Ιανουαρίου 2014. Ανακτήθηκε στις 21 Ιανουαρίου 2019.

uniprot.org

Universal protein resource accession number Q8WVJ9 for "TWIST2 – Twist-related protein 2 – Homo sapiens (Human) – TWIST2 gene & protein " στο UniProt.