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External ear malformations: epidemiology, genetics, and natural history.

作者信息

Melnick M, Myrianthopoulos N C, Paul N W

出版信息

Birth Defects Orig Artic Ser. 1979;15(9):i-ix, 1-140.

PMID:393325
Abstract
摘要

相似文献

1
External ear malformations: epidemiology, genetics, and natural history.
Birth Defects Orig Artic Ser. 1979;15(9):i-ix, 1-140.
2
[Malformations in otorhinolaryngology. Genetic report].
Arch Klin Exp Ohren Nasen Kehlkopfheilkd. 1972;202(2):253-62.
3
[Human genetic counseling. I. Incidence, etiology and risk in repetion of congenital malformations].[人类遗传咨询。I. 先天性畸形复发中的发病率、病因及风险]
Zentralbl Gynakol. 1974 Mar 1;96(9):257-66.
4
Genetic counseling.遗传咨询
Trans Am Acad Ophthalmol Otolaryngol. 1972 Sep-Oct;76(5):1203-13.
5
[External ear abnormalities: syndromic and genetic aspects].[外耳畸形：综合征及遗传学方面]
Rev Laryngol Otol Rhinol (Bord). 1997;118(1):5-10.
6
Association of hypertelorism and hypospadias--the BBB-syndrome.眼距过宽与尿道下裂的关联——BBB综合征
Helv Paediatr Acta. 1972 Dec;27(6):575-81.
7
Genetics for the clinical obstetrician-gynecologist.临床妇产科医生的遗传学
Obstet Gynecol Annu. 1980;9:1-53.
8
Genetics of common congenital malformations in man.人类常见先天性畸形的遗传学
Proc R Soc Med. 1976 Jan;69(1):38-40. doi: 10.1177/003591577606900120.
9
Phenotype and counseling in lacrimo-auriculo-dento-digital (LADD) syndrome.泪腺-耳-齿-指（LADD）综合征的表型与遗传咨询
Genet Couns. 1993;4(4):305-9.
10
LADD syndrome in five members of a three-generation family and prenatal diagnosis.
Genet Couns. 1994;5(1):85-91.

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1
[Selection and application in the approach of Bonebridge implantation for bilateral congenital malformation of external and middle ear: selection and application].[骨桥植入术在双侧先天性中耳和外耳畸形治疗中的选择与应用：选择与应用]
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2021 Jul;35(7):602-607. doi: 10.13201/j.issn.2096-7993.2021.07.006.
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Anatomical variants of the superficial temporal artery in patients with microtia: a pilot descriptive study.小耳畸形患者颞浅动脉的解剖变异：一项初步描述性研究。
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3
Characterizing facial features in individuals with craniofacial microsomia: A systematic approach for clinical research.
颅面短小畸形个体面部特征的表征：一种临床研究的系统方法。
Birth Defects Res A Clin Mol Teratol. 2016 Nov;106(11):915-926. doi: 10.1002/bdra.23560.
4
Prenatal ultrasound screening for external ear abnormality in the fetuses.胎儿外耳道异常的产前超声筛查。
Biomed Res Int. 2014;2014:357564. doi: 10.1155/2014/357564. Epub 2014 Jun 23.
5
Non-inherited manifestation of bilateral branchial fistulae, bilateral pre-auricular sinuses and bilateral hearing loss: A variant of branchio-oto-renal syndrome.双侧鳃裂瘘管、双侧耳前窦道及双侧听力损失的非遗传性表现：鳃-耳-肾综合征的一种变异型
Indian J Otolaryngol Head Neck Surg. 2005 Jan;57(1):52-4. doi: 10.1007/BF02907630.
6
Hemifacial microsomia: from gestation to childhood.半侧颜面短小畸形：从孕期到儿童期
J Craniofac Surg. 2009 Mar;20 Suppl 1(Suppl 1):664-9. doi: 10.1097/SCS.0b013e318193d5d5.
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Causation of permanent unilateral and mild bilateral hearing loss in children.儿童永久性单侧和轻度双侧听力损失的病因
Trends Amplif. 2008 Mar;12(1):17-25. doi: 10.1177/1084713807313085.
8
Definition of a critical region on chromosome 18 for congenital aural atresia by arrayCGH.通过阵列比较基因组杂交技术确定18号染色体上先天性耳道闭锁关键区域的定义。
Am J Hum Genet. 2003 Jun;72(6):1578-84. doi: 10.1086/375695. Epub 2003 May 9.
9
Branchio-oto-renal (BOR) syndrome: variable expressivity in a five-generation pedigree.
Eur J Pediatr. 1994 Jun;153(6):446-50. doi: 10.1007/BF01983410.
10
Tomography of neonates with abnormal ears.耳部异常新生儿的体层摄影术。
Arch Dis Child. 1980 Oct;55(10):828. doi: 10.1136/adc.55.10.828-b.