白兰地酒分离株的医学和牙科检查结果。 - Suppr

Suppr

超能文献

Medical and dental findings in the Brandywine isolate.

作者信息

Witkop C J, MacLean C J, Schmidt P J, Henry J L

出版信息

Ala J Med Sci. 1966 Oct;3(4):382-403.

PMID:5978170

Abstract

摘要

相似文献

Medical and dental findings in the Brandywine isolate.白兰地酒分离株的医学和牙科检查结果。

Ala J Med Sci. 1966 Oct;3(4):382-403.

An unusual presentation of opalescent dentin and Brandywine isolate hereditary opalescent dentin in an Ashkenazic Jewish family.一个阿什肯纳兹犹太家庭中出现的乳光牙本质和布兰迪万分离株遗传性乳光牙本质的不寻常表现。

Oral Surg Oral Med Oral Pathol. 1985 Jun;59(6):608-15. doi: 10.1016/0030-4220(85)90190-2.

Dentinogenesis imperfecta traceable through five generations of a part American Indian family.在一个部分为美国印第安人的家族中，牙本质发育不全可追溯五代。

Oral Surg Oral Med Oral Pathol. 1973 Feb;35(2):180-6. doi: 10.1016/0030-4220(73)90283-1.

Dentinogenesis imperfecta in the Brandywine isolate (DI type III): clinical, radiologic, and scanning electron microscopic studies of the dentition.白兰地酒分离株中的牙本质发育不全（III型牙本质发育不全）：牙列的临床、放射学和扫描电子显微镜研究

Oral Surg Oral Med Oral Pathol. 1983 Sep;56(3):267-74. doi: 10.1016/0030-4220(83)90008-7.

Sibling similarities in dental caries.

J Dent Res. 1976 Sep-Oct;55(5):914. doi: 10.1177/00220345760550053801.

Genetic linkage of the dentinogenesis imperfecta type III locus to chromosome 4q.III型牙本质发育不全基因座与4号染色体长臂的遗传连锁

J Dent Res. 1999 Jun;78(6):1277-82. doi: 10.1177/00220345990780061301.

Total sucrose intake and dental caries in black and white South African children of 1-6 years. Part II: dental caries and sucrose intake.

J Dent Assoc S Afr. 1978 Oct;33(10):539-44.

Dentinogenesis imperfecta: genetic variations in a six-generation family.牙本质发育不全：一个六代家族中的基因变异

J Dent Res. 1969 Nov-Dec;48(6):1196-9. doi: 10.1177/00220345690480061701.

Rampant caries and labial caries--synonyms?

S Afr Med J. 1977 Oct 1;52(15):594.

Dentinogenesis imperfecta.牙本质发育不全

Int J Orthod. 1973 Mar;11(1):11-6.

引用本文的文献

Dentinogenesis imperfecta in a 6-year-old male neutered Labrador retriever: Case report with atypical clinical presentation and treatment review.一只6岁去势雄性拉布拉多寻回犬的牙本质发育不全：具有非典型临床表现和治疗回顾的病例报告

Front Vet Sci. 2024 Nov 4;11:1473390. doi: 10.3389/fvets.2024.1473390. eCollection 2024.

The Modified Shields Classification and 12 Families with Defined Mutations.改良的 Shields 分类与 12 个明确突变家族。

Genes (Basel). 2022 May 12;13(5):858. doi: 10.3390/genes13050858.

The dentin phosphoprotein repeat region and inherited defects of dentin.牙本质磷蛋白重复区域与牙本质遗传性缺陷

Mol Genet Genomic Med. 2015 Sep 7;4(1):28-38. doi: 10.1002/mgg3.176. eCollection 2016 Jan.

Hereditary opalescent dentin.遗传性乳光牙本质

BMJ Case Rep. 2013 Apr 3;2013:bcr2013008958. doi: 10.1136/bcr-2013-008958.

Phenotype characterization and DSPP mutational analysis of three Brazilian dentinogenesis imperfecta type II families.三个巴西II型牙本质发育不全家族的表型特征及DSPP突变分析

Cells Tissues Organs. 2009;189(1-4):230-6. doi: 10.1159/000152917. Epub 2008 Sep 16.

Consanguinity and blood group distribution in an Amish Isolate.阿米什人隔离群体中的近亲关系与血型分布

Am J Hum Genet. 1968 Nov;20(6):522-7.

Autosomal recessive oculocutaneous albinism in man. Evidence for genetic heterogeneity.人类常染色体隐性眼皮肤白化病。遗传异质性的证据。

Am J Hum Genet. 1970 Jan;22(1):55-74.

Oral clefts in the American Indian.美洲印第安人的唇腭裂。

Public Health Rep (1896). 1967 Sep;82(9):807-12.

文献检索

告别复杂PubMed语法，用中文像聊天一样搜索，搜遍4000万医学文献。AI智能推荐，让科研检索更轻松。

立即免费搜索

文件翻译

保留排版，准确专业，支持PDF/Word/PPT等文件格式，支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述，25分钟生成高质量综述，智能提取关键信息，辅助科研写作。

立即免费体验