PubMed for id: 91261

Year	Number of Results
1976	1
1978	2
1979	1
1980	2
1982	1
1983	3
1984	1
1985	2
1986	2
1987	2
1988	1
1989	2
1990	1
1991	3
1992	5
1993	2
1994	5
1995	7
1996	6
1997	4
1998	12
1999	7
2000	9
2001	9
2002	6
2003	5
2004	7
2005	6
2006	14
2007	7
2008	11
2009	15
2010	10
2011	12
2012	15
2013	15
2014	16
2015	15
2016	14
2017	8
2018	18
2019	12
2020	13
2021	15
2022	20
2023	15
2024	5

1

A Heterozygous Novel Mutation in TFAP2A Gene Causes Atypical Branchio-Oculo-Facial Syndrome With Isolated Coloboma of Choroid: A Case Report.

Min J, Mao B, Wang Y, He X, Gao S, Wang H. Min J, et al. Front Pediatr. 2020 Jul 17;8:380. doi: 10.3389/fped.2020.00380. eCollection 2020. Front Pediatr. 2020. PMID: 32766183 Free PMC article.

2

A Rare Case of Branchio-oculo-facial Syndrome: Clinical and Histopathological Features.

Iraji F, Shahbazi M, Abtahi-Naeini B, Asilian A, Shahmoradi Z, Bostakian A, Rajabi P, Kazemipour S. Iraji F, et al. Adv Biomed Res. 2018 Nov 27;7:145. doi: 10.4103/abr.abr_31_18. eCollection 2018. Adv Biomed Res. 2018. PMID: 30596055 Free PMC article.

3

Novel TFAP2A mutation in a Japanese family with Branchio-oculo-facial syndrome.

Sato T, Samura O, Kato N, Taniguchi K, Takahashi K, Ito Y, Aoki H, Kobayashi M, Migita O, Okamoto A, Hata K. Sato T, et al. Hum Genome Var. 2018 May 10;5:5. doi: 10.1038/s41439-018-0004-z. eCollection 2018. Hum Genome Var. 2018. PMID: 29760939 Free PMC article.

4

An Unconventional Presentation of Branchio-Oculo-Facial Syndrome.

Yi S, Albino FP, Wood BC, Sauerhammer TM, Rogers GF, Oh AK. Yi S, et al. J Craniofac Surg. 2016 Sep;27(6):1412-4. doi: 10.1097/SCS.0000000000002813. J Craniofac Surg. 2016. PMID: 27607113

5

[New oral manifestations of Branchio-oculo-facial syndrome. Case report].

García Flores JB, Escamilla Ocañas CE, Martínez Menchaca HR, Treviño Alanís MG, Rivera Silva G. García Flores JB, et al. Arch Argent Pediatr. 2015 Jan;113(1):e14-6. doi: 10.5546/aap.2015.e14. Arch Argent Pediatr. 2015. PMID: 25622170 Free article. Spanish.

6

A clinical and molecular analysis of branchio-oculo-facial syndrome patients in Russia revealed new mutations in TFAP2A.

Meshcheryakova TI, Zinchenko RA, Vasilyeva TA, Marakhonov AV, Zhylina SS, Petrova NV, Kozhanova TV, Belenikin MS, Petrin AN, Mutovin GR. Meshcheryakova TI, et al. Ann Hum Genet. 2015 Mar;79(2):148-52. doi: 10.1111/ahg.12098. Epub 2015 Jan 15. Ann Hum Genet. 2015. PMID: 25590586

7

Branchio-oculo-facial syndrome: a three generational family with markedly variable phenotype including neonatal lethality.

Titheradge HL, Patel C, Ragge NK. Titheradge HL, et al. Clin Dysmorphol. 2015 Jan;24(1):13-6. doi: 10.1097/MCD.0000000000000056. Clin Dysmorphol. 2015. PMID: 25325185

8

Branchio-oculo-facial syndrome in a newborn caused by a novel TFAP2A mutation.

Günes N, Cengiz FB, Duman D, Dervişoğlu S, Tekin M, Tüysüz B. Günes N, et al. Genet Couns. 2014;25(1):41-7. Genet Couns. 2014. PMID: 24783654

9

Analysis of TFAP2A mutations in Branchio-Oculo-Facial Syndrome indicates functional complexity within the AP-2α DNA-binding domain.

Li H, Sheridan R, Williams T. Li H, et al. Hum Mol Genet. 2013 Aug 15;22(16):3195-206. doi: 10.1093/hmg/ddt173. Epub 2013 Apr 10. Hum Mol Genet. 2013. PMID: 23578821 Free PMC article.

10

A family with a complex clinical presentation characterized by arrhythmogenic right ventricular dysplasia/cardiomyopathy and features of branchio-oculo-facial syndrome.

Murray B, Wagle R, Amat-Alarcon N, Wilkens A, Stephens P, Zackai EH, Goldmuntz E, Calkins H, Deardorff MA, Judge DP. Murray B, et al. Am J Med Genet A. 2013 Feb;161A(2):371-6. doi: 10.1002/ajmg.a.35733. Epub 2013 Jan 10. Am J Med Genet A. 2013. PMID: 23307527

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