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Electron optic microanalysis of two gene products in enamel of females heterozygous for X-linked hypomaturation amelogenesis imperfecta.

作者信息

Sauk J J, Lyon H W, Witkop C J

出版信息

Am J Hum Genet. 1972 May;24(3):267-76.

PMID:4623931
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1762280/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5569/1762280/d4b8c97b38f7/ajhg00454-0038-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5569/1762280/35b42079110e/ajhg00454-0034-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5569/1762280/91e9c0b6a6b0/ajhg00454-0035-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5569/1762280/8295547af762/ajhg00454-0037-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5569/1762280/d4b8c97b38f7/ajhg00454-0038-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5569/1762280/35b42079110e/ajhg00454-0034-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5569/1762280/91e9c0b6a6b0/ajhg00454-0035-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5569/1762280/8295547af762/ajhg00454-0037-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5569/1762280/d4b8c97b38f7/ajhg00454-0038-a.jpg

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Electron optic microanalysis of two gene products in enamel of females heterozygous for X-linked hypomaturation amelogenesis imperfecta.对X连锁低成熟型牙釉质发育不全女性杂合子牙釉质中两种基因产物的电子光学显微分析。
Am J Hum Genet. 1972 May;24(3):267-76.
2
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Amelogenesis imperfecta: Report of a case and review of literature.牙釉质发育不全:1例报告及文献复习
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A large X-chromosomal deletion is associated with microphthalmia with linear skin defects (MLS) and amelogenesis imperfecta (XAI).

本文引用的文献

1
HEREDITARY ENAMEL DEFECTS.遗传性牙釉质缺陷
Proc R Soc Med. 1964 Jan;57(1):53-8. doi: 10.1177/003591576405700112.
2
Gene action in the X-chromosome of the mouse (Mus musculus L.).小鼠(小家鼠)X染色体上的基因作用。
Nature. 1961 Apr 22;190:372-3. doi: 10.1038/190372a0.
3
Hereditary defects in enamel and dentin.牙釉质和牙本质的遗传性缺陷。
一个大的X染色体缺失与小眼症合并线性皮肤缺损(MLS)和牙釉质发育不全(XAI)相关。
Am J Med Genet A. 2009 Aug;149A(8):1698-705. doi: 10.1002/ajmg.a.32968.
4
Partial rescue of the amelogenin null dental enamel phenotype.釉原蛋白缺失型牙釉质表型的部分挽救。
J Biol Chem. 2008 May 30;283(22):15056-62. doi: 10.1074/jbc.M707992200. Epub 2008 Apr 3.
5
Ultrastructural study of amelogenesis imperfecta.
Calcif Tissue Res. 1977 Dec 28;24(2):191-7. doi: 10.1007/BF02223315.
Acta Genet Stat Med. 1957;7(1):236-9. doi: 10.1159/000150974.
4
[Hereditary structural abnormalities of human teeth].
Acta Genet Stat Med. 1957;7(1):231-5.
5
The development of enamel structure.牙釉质结构的发育
Proc R Soc Med. 1967 Sep;60(9):923-8. doi: 10.1177/003591576706000965.
6
Electron probe microanalysis of noncarious enamel and dentin and calcified tissues in mottled teeth.
J Dent Res. 1969 Jan-Feb;48(1):131-9. doi: 10.1177/00220345690480010501.
7
Partial expression of sex-linked recessive amelogenesis imperfecta in females compatible with the Lyon hypothesis.与莱昂假说相符的女性性连锁隐性遗传性釉质发育不全的部分表现。
Oral Surg Oral Med Oral Pathol. 1967 Feb;23(2):174-82. doi: 10.1016/0030-4220(67)90092-8.
8
Scanning electron microscope studies of EDTA-treated enamel.经乙二胺四乙酸处理的牙釉质的扫描电子显微镜研究。
J Dent Res. 1969 Nov-Dec;48(6):1234-42. doi: 10.1177/00220345690480062501.
9
Scanning electron microscope studies of dental enamel.牙釉质的扫描电子显微镜研究。
J Dent Res. 1969 Mar-Apr;48(2):242-50. doi: 10.1177/00220345690480021301.
10
The effects of different demineralizing agents on human enamel surfaces studied by scanning electron microscopy.通过扫描电子显微镜研究不同脱矿剂对人牙釉质表面的影响。
Arch Oral Biol. 1967 Dec;12(12):1621-34. doi: 10.1016/0003-9969(67)90196-3.