101 related articles for article (PubMed ID: 34589676)
1. Identification of potential pathogenic mutations in Chinese children with first branchial cleft anomalies detected by whole-exome sequencing.
Yang Y; Liu W; Jin Y; Chen M; Lu J; Yu Y; Ren H; Han S; Chu P; Guo Y; Zhang J; Ni X
Pediatr Investig; 2021 Sep; 5(3):211-216. PubMed ID: 34589676
[TBL] [Abstract][Full Text] [Related]
2. Clinical analysis of first branchial cleft anomalies in children.
Liu W; Liu B; Chen M; Hao J; Yang Y; Zhang J
Pediatr Investig; 2018 Sep; 2(3):149-153. PubMed ID: 32851251
[TBL] [Abstract][Full Text] [Related]
3. Clinical Analysis of Type II First Branchial Cleft Anomalies in Children.
Liu W; Chen M; Liu B; Zhang J; Ni X
Laryngoscope; 2021 Apr; 131(4):916-920. PubMed ID: 32846011
[TBL] [Abstract][Full Text] [Related]
4. The treatment for the first branchial cleft anomalies in children.
Liu W; Chen M; Hao J; Yang Y; Zhang J; Ni X
Eur Arch Otorhinolaryngol; 2017 Sep; 274(9):3465-3470. PubMed ID: 28634783
[TBL] [Abstract][Full Text] [Related]
5. First Brachial Cleft Anomalies in Children: An Innovative Surgical Technique Preventing External Auditory Canal Stenosis.
Kotowski M; Szydlowski J
Children (Basel); 2023 Jul; 10(7):. PubMed ID: 37508655
[TBL] [Abstract][Full Text] [Related]
6. Analysis of the Clinical Features and Surgical Outcomes of First Branchial Cleft Anomalies.
Yang R; Dong C; Chen Y; Liu H; Zhang C; Lai Y; Zha D; Han Y
Laryngoscope; 2022 May; 132(5):1008-1014. PubMed ID: 34617600
[TBL] [Abstract][Full Text] [Related]
7. Identification of susceptibility genes in non-syndromic cleft lip with or without cleft palate using whole-exome sequencing.
Liu YP; Xu LF; Wang Q; Zhou XL; Zhou JL; Pan C; Zhang JP; Wu QR; Li YQ; Xia YJ; Peng X; Zhang MR; Yu HM; Xu LC
Med Oral Patol Oral Cir Bucal; 2015 Nov; 20(6):e763-70. PubMed ID: 26449438
[TBL] [Abstract][Full Text] [Related]
8. The Treatment for Type II First Branchial Cleft Anomalies With Abnormalities Lateral to the Tympanic Membrane.
Liu W; Chen M; Yang Y; Shao J; Ni X; Zhang J
Ear Nose Throat J; 2022 Dec; ():1455613221147344. PubMed ID: 36542778
[TBL] [Abstract][Full Text] [Related]
9. Identification of novel mutations in endometrial cancer patients by whole-exome sequencing.
Chang YS; Huang HD; Yeh KT; Chang JG
Int J Oncol; 2017 May; 50(5):1778-1784. PubMed ID: 28339086
[TBL] [Abstract][Full Text] [Related]
10. First branchial cleft anomalies in children: Experience with 30 cases.
Li W; Zhao L; Xu H; Li X
Exp Ther Med; 2017 Jul; 14(1):333-337. PubMed ID: 28672934
[TBL] [Abstract][Full Text] [Related]
11. Unusual presentation of a first branchial arch fistula with maxillofacial infection: a case report.
Han Y; Yang RQ; Hong L; Zhong CP; Zha DJ
BMC Surg; 2021 Jul; 21(1):306. PubMed ID: 34217239
[TBL] [Abstract][Full Text] [Related]
12. Differences in management outcome for first branchial cleft anomalies: A comparison of infants and toddlers to older children.
Brown LA; Johnston DR; Rastatter J; Sweis BM; Maddalozzo J
Int J Pediatr Otorhinolaryngol; 2019 Jul; 122():161-164. PubMed ID: 31029951
[TBL] [Abstract][Full Text] [Related]
13. First branchial cleft anomaly: clinical insight into its relevance in otolaryngology with pediatric considerations.
Maithani T; Pandey A; Dey D; Bhardwaj A; Singh VP
Indian J Otolaryngol Head Neck Surg; 2014 Jan; 66(Suppl 1):271-6. PubMed ID: 24533397
[TBL] [Abstract][Full Text] [Related]
14. A Case of First Branchial Cleft Fistula Presenting with an External Opening on the Root of the Helical Crus.
Cho SI
Case Rep Med; 2018; 2018():4215802. PubMed ID: 29560006
[TBL] [Abstract][Full Text] [Related]
15. [Congenital microtia with aural atresia or stenosis accompany with first branchial cleft anomaly: report of 5 cases].
Dou JM; Wang DN; Zhao SQ; Li Y; Ma XB; Chen PW; Yang JS
Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2019 May; 54(5):349-354. PubMed ID: 31137094
[No Abstract] [Full Text] [Related]
16. Branchial anomalies in children.
Bajaj Y; Ifeacho S; Tweedie D; Jephson CG; Albert DM; Cochrane LA; Wyatt ME; Jonas N; Hartley BE
Int J Pediatr Otorhinolaryngol; 2011 Aug; 75(8):1020-3. PubMed ID: 21680029
[TBL] [Abstract][Full Text] [Related]
17. Concurrent exome-targeted next-generation sequencing and single nucleotide polymorphism array to identify the causative genetic aberrations of isolated Mayer-Rokitansky-Küster-Hauser syndrome.
Chen MJ; Wei SY; Yang WS; Wu TT; Li HY; Ho HN; Yang YS; Chen PL
Hum Reprod; 2015 Jul; 30(7):1732-42. PubMed ID: 25924657
[TBL] [Abstract][Full Text] [Related]
18. First branchial cleft anomalies: otologic manifestations and treatment outcomes.
Shinn JR; Purcell PL; Horn DL; Sie KC; Manning SC
Otolaryngol Head Neck Surg; 2015 Mar; 152(3):506-12. PubMed ID: 25524898
[TBL] [Abstract][Full Text] [Related]
19. First branchial cleft cyst accompanied by external auditory canal atresia and middle ear malformation: A case report.
Zhang CL; Li CL; Chen HQ; Sun Q; Liu ZH
World J Clin Cases; 2020 Aug; 8(16):3616-3620. PubMed ID: 32913872
[TBL] [Abstract][Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]
