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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1977 1
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PubMed for id: 767161

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Page 1
Expansion of the phenotypic and mutational spectrum of Carpenter syndrome.
Khairat R, Elhossini R, Sobreira N, Wohler E, Otaify G, Mohamed AM, Abdel Raouf ER, Sayed I, Aglan M, Ismail S, Temtamy SA. Khairat R, et al. Eur J Med Genet. 2022 Jan;65(1):104377. doi: 10.1016/j.ejmg.2021.104377. Epub 2021 Nov 5. Eur J Med Genet. 2022. PMID: 34748996
Complex craniosynostosis in the context of Carpenter's syndrome.
Bouaré F, Noureldine MHA, Hajhouji F, Ghannane H, Jallo GI, Ait Benali S. Bouaré F, et al. Childs Nerv Syst. 2022 Apr;38(4):831-835. doi: 10.1007/s00381-021-05288-4. Epub 2021 Jul 9. Childs Nerv Syst. 2022. PMID: 34244844
Thyroid autoimmunity and polyglandular endocrine syndromes.
Wémeau JL, Proust-Lemoine E, Ryndak A, Vanhove L. Wémeau JL, et al. Hormones (Athens). 2013 Jan-Mar;12(1):39-45. doi: 10.1007/BF03401285. Hormones (Athens). 2013. PMID: 23624130 Free article. Review.
Mutations in multidomain protein MEGF8 identify a Carpenter syndrome subtype associated with defective lateralization.
Twigg SR, Lloyd D, Jenkins D, Elçioglu NE, Cooper CD, Al-Sannaa N, Annagür A, Gillessen-Kaesbach G, Hüning I, Knight SJ, Goodship JA, Keavney BD, Beales PL, Gileadi O, McGowan SJ, Wilkie AO. Twigg SR, et al. Am J Hum Genet. 2012 Nov 2;91(5):897-905. doi: 10.1016/j.ajhg.2012.08.027. Epub 2012 Oct 11. Am J Hum Genet. 2012. PMID: 23063620 Free PMC article.
Carpenter syndrome: a case report.
Begum S, Khatun N, Rayhan SM, Rahman SA. Begum S, et al. Mymensingh Med J. 2012 Jul;21(3):547-9. Mymensingh Med J. 2012. PMID: 22828559
14 results