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[1]肖智祥,康映泉,何少華,等.兒童Apert綜合征1例報(bào)告[J].福建醫(yī)藥雜志,2021,43(06):178-179.
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兒童Apert綜合征1例報(bào)告()
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《福建醫(yī)藥雜志》[ISSN:1002-2600/CN:35-1071/R]

卷:
43
期數(shù):
2021年06期
頁碼:
178-179
欄目:
病例報(bào)告
出版日期:
2021-12-15

文章信息/Info

作者:
肖智祥康映泉何少華徐迪李鋆
福建醫(yī)科大學(xué)省立臨床醫(yī)學(xué)院 福建省立醫(yī)院小兒外科(福州 350001)

參考文獻(xiàn)/References:

[1] Munarriz P M, Pascual B,Castaño-Leon A M, et al.Apert syndrome: Cranial procedures and brain malformations in a series of patients[J].Surg Neurol Int,2020, 11(361):1-8.
[2] Pius S, Ibrahim H A, Bello M, et al.Apert Syndrome: A case report and review of literature[J].Open Journal of Pediatrics,2016, 6(2):175-184.
[3] 王立丹,黃穗,劉帆, 等.Apert綜合征2例[J].中華實(shí)用兒科臨床雜志,2016,31(20):1584-1585.
[4] Allanson J E.Germinal mosaieism in Apart syndrome[J].Clin Genet,1986,29(5):429-433.
[5] Goyal M, Gupta A, Kapoor S, et al.Apert syndrome with preaxial polydactyly with FGFR2 gene mutation[J].The Indian Journal of Pediatrics,2020, 87(6):469-470.
[6] Raposo-Amaral C E, Zecchin K G, Denadai R, et al.Paternal age as a contributing factor in apert syndrome[J].Journal of Craniofacial Surgery,2020, 31(4):1167-1167.
[7] Oldridge M,Zackai E H,McDonald-McGinn D M,et al.De novo aluelement insertions in FGFR2 identify a distinct pathological basis for Apert syndrome[J].Am J Hum Genet,1999,64(2):446-461.
[8] Upton J. Apert syndrome.Classification and pathologic anatomy of limb anomalies[J].Clin Plast Surg, 1991, 18(2):321-55.
[9] Raposo-Amaral C E, Denadai R, Furlan P, et al.Treatment of apert hand syndrome: strategies for achieving a five-digit hand[J].Plastic and Reconstructive Surgery, 2018, 142(4):972-982.
[10] Kobayashi Y, Ogura K, Hikita R, et al.Craniofacial, oral, and cervical morphological characteristics in Japanese patients with Apert syndrome or Crouzon syndrome[J].European journal of orthodontics,2021,43(1):36-44.
[11] 周潔,鄧永鍵,司馬雪琴, 等.胎兒Apert綜合征1例尸檢及文獻(xiàn)匯報(bào)[J].南方醫(yī)科大學(xué)學(xué)報(bào),2011,31(3):557-558.

更新日期/Last Update: 2021-12-15