[1] |
Balamotis, M.A., Pennella, M.A., Stevens, J.L., Wasylyk, B., Belmont, A.S., Berk, A.J., 2009. Complexity in transcription control at the activation domain-mediator interface. Sci. Signal. 2, ra20.
|
[2] |
Chen, C.-P., Huang, H.-K., Liu, Y.-P., Chern, S.-R., Su, J.-W., Wang, W., 2013. Pfeiffer syndrome with FGFR2 W290C mutation perinatally presenting extreme proptosis. Taiwan. J. Obstet. Gynecol. 52, 607-610.
|
[3] |
Goos, J.A.C., Mathijssen, I.M.J., 2019. Genetic causes of craniosynostosis: an update. Mol. Syndromol. 10, 6-23.
|
[4] |
Kan, S., Elanko, N., Johnson, D., Cornejo-Roldan, L., Cook, J., Reich, E.W., Tomkins, S., Verloes, A., Twigg, S.R.F., Rannan-Eliya, S., et al, 2002. Genomic screening of fibroblast growth-factor receptor 2 reveals a wide spectrum of mutations in patients with syndromic craniosynostosis. Am. J. Hum. Genet. 70, 472-486.
|
[5] |
Ke, R., Yang, X., Ge, M., Cai, T., Lei, J., Mu, X., 2015. S267P mutation in FGFR2: first report in a patient with Crouzon syndrome. J. Craniofac. Surg. 23, 592-594.
|
[6] |
Ko, J.M., Jeong, S.-Y., Yang, J.-A., Park, D.H., Yoon, S.H., 2012. Molecular genetic analysis of TWIST1 and FGFR3 genes in Korean patients with coronal synostosis: identification of three novel TWIST1 mutations. Plast. Reconstr. Surg. 129, 814e-821e.
|
[7] |
Lajeunie, E., Heuertz, S., El Ghouzzi, V., Martinovic, J., Renier, D., Le Merrer, M., Bonaventure, J., 2006. Mutation screening in patients with syndromic craniosynostoses indicates that a limited number of recurrent FGFR2 mutations accounts for severe forms of Pfeiffer syndrome. Eur. J. Hum. Genet. 14, 289-298.
|
[8] |
Lattanzi, W., Barba, M., Di Pietro, L., Boyadjiev, S.A., 2017. Genetic advances in craniosynostosis. Am. J. Med. Genet. A. 173, 1406-1429.
|
[9] |
Lee, E., Le, T., Zhu, Y., Elakis, G., Turner, A., Lo, W., Venselaar, H., Verrenkamp, C.-A., Snow, N., Mowat, D., et al, 2018. A craniosynostosis massively parallel sequencing panel study in 309 Australian and New Zealand patients: findings and recommendations. Genet. Med. 20, 1061-1068.
|
[10] |
Lenton, K.A., Nacamuli, R.P., Wan, D.C., Helms, J.A., Longaker, M.T., 2005. Cranial Suture Biology. Curr. Top. Dev. Biol. 66: 287-328.
|
[11] |
Loeys, B.L., Chen, J., Neptune, E.R., Judge, D.P., Podowski, M., Holm, T., Meyers, J., Leitch, C.C., Katsanis, N., Sharifi, N., et al, 2005. A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2. Nat. Genet. 37, 275-281.
|
[12] |
Paumard-Hernandez, B., Berges-Soria, J., Barroso, E., Rivera-Pedroza, C.I., Perez-Carrizosa, V., Benito-Sanz, S., Lopez-Messa, E., Santos, F., Garcia-Recuero, I.I., Romance, A., et al, 2015. Expanding the mutation spectrum in 182 Spanish probands with craniosynostosis: identification and characterization of novel TCF12 variants. Eur. J. Hum. Genet. 23, 907-914.
|
[13] |
Powers, C.J., McLeskey, S.W., Wellstein, A., 2000. Fibroblast growth factors, their receptors and signaling. Endocr. Relat. Cancer 165-197.
|
[14] |
Priolo, M., Lerone, M., Baffico, M., Baldi, M., Ravazzolo, R., Cama, A., Capra, V., Silengo, M., 2000. Pfeiffer syndrome type 2 associated with a single amino acid deletion in the PGFR2 gene. Clin. Genet. 58, 81-83.
|
[15] |
Roscioli, T., Elakis, G., Cox, T.C., Moon, D.J., Venselaar, H., Turner, A.M., Le, T., Hackett, E., Haan, E., Colley, A., et al, 2013. Genotype and clinical care correlations in craniosynostosis: findings from a cohort of 630 Australian and New Zealand patients. Am. J. Med. Genet. C Semin. Med. Genet. 163, 259-270.
|
[16] |
Shotelersuk, V., Ittiwut, C., Srivuthana, S., Mahatumarat, C., Lerdlum, S., Wacharasindhu, S., 2002. Distinct craniofacial-skeletal-dermatological dysplasia in a patient with W290C mutation inFGFR2. Am. J. Med. Genet. 113, 4-8.
|
[17] |
Richards, S., Aziz, N., Bale, S., Bick, D., Das, S., Gastier-Foster, J., Grody, W.W., Hegde, M., Lyon, E., Spector, E., Voelkerding, K., Rehm, H.L., 2015. ACMG Laboratory Quality Assurance Committee. Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology. Genet Med. 17, 405-424.
|
[18] |
Unolt, M., Kammoun, M., Nowakowska, B., Graham, G.E., Crowley, T.B., Hestand, M.S., Demaerel, W., Geremek, M., Emanuel, B.S., Zackai, E.H., et al, 2020. Pathogenic variants in CDC45 on the remaining allele in patients with a chromosome 22q11.2 deletion result in a novel autosomal recessive condition. Genet. Med. 22, 326-335.
|
[19] |
Wilkie, A.O.M., Byren, J.C., Hurst, J.A., Jayamohan, J., Johnson, D., Knight, S.J.L., Lester, T., Richards, P.G., Twigg, S.R.F., Wall, S.A., 2010. Prevalence and complications of single-gene and chromosomal disorders in craniosynostosis. Pediatrics 126, e391-e400.
|
[20] |
Wilkie, A.O.M., Johnson, D., Wall, S.A., 2017. Clinical genetics of craniosynostosis: Curr. Opin. Pediatr. 29, 622-628.
|