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

Year Number of Results
1967 1
2000 2
2001 1
2002 2
2003 1
2004 1
2005 3
2006 3
2007 1
2008 4
2009 4
2010 6
2011 8
2012 5
2013 8
2014 5
2015 6
2016 2
2017 2
2018 5
2019 4
2020 1
2021 4
2022 1
2024 0

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PubMed for Bookshelf ID: 3072110

66 results

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Page 1
[Brain-lung-thyroid syndrome in a newborn with deletion 14q12-q21.1].
Villamil-Osorio M, Yunis LK, Quintero L, Restrepo-Gualteros S, Yunis JJ, Jaramillo L, Agudelo BI, Ladino Y. Villamil-Osorio M, et al. Andes Pediatr. 2021 Dec;92(6):930-936. doi: 10.32641/andespediatr.v92i6.3287. Epub 2021 Nov 5. Andes Pediatr. 2021. PMID: 35506806 Free article. Spanish.
Deletion of conserved non-coding sequences downstream from NKX2-1: A novel disease-causing mechanism for benign hereditary chorea.
Liao J, Coffman KA, Locker J, Padiath QS, Nmezi B, Filipink RA, Hu J, Sathanoori M, Madan-Khetarpal S, McGuire M, Schreiber A, Moran R, Friedman N, Hoffner L, Rajkovic A, Yatsenko SA, Surti U. Liao J, et al. Mol Genet Genomic Med. 2021 Apr;9(4):e1647. doi: 10.1002/mgg3.1647. Epub 2021 Mar 5. Mol Genet Genomic Med. 2021. PMID: 33666368 Free PMC article.
Chiari Malformation Type I in a Patient with a Novel NKX2-1 Mutation.
Gonçalves D, Lourenço L, Guardiano M, Castro-Correia C, Sampaio M, Leão M. Gonçalves D, et al. J Pediatr Neurosci. 2019 Jul-Sep;14(3):169-172. doi: 10.4103/jpn.JPN_108_18. Epub 2019 Sep 27. J Pediatr Neurosci. 2019. PMID: 31649781 Free PMC article.
66 results