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A new estimate of the achondroplasia mutation rate.

作者信息

Gardner R J

出版信息

Clin Genet. 1977 Jan;11(1):31-8. doi: 10.1111/j.1399-0004.1977.tb01274.x.

DOI:10.1111/j.1399-0004.1977.tb01274.x
PMID:830446
Abstract

An estimate is derived of the mutation of achondroplasia based upon the accumulated data of recent newborn studies in four cities. In a total of 242,257 births, seven infants had mutant achondroplasia, the diagnosis being confirmed radiologically in all but one. From this, the rate of mutation of the normal to the achondroplasia allele is calculated to be 1.4 x 10(-5) +/- standard error 0.5 x 10(-5). Certain shortcomings of this estimate are discussed.

摘要

相似文献

1
A new estimate of the achondroplasia mutation rate.
Clin Genet. 1977 Jan;11(1):31-8. doi: 10.1111/j.1399-0004.1977.tb01274.x.
2
[The so-called chondrodystrophia of the newborn (author's transl)].[所谓新生儿软骨营养障碍(作者译)]
Radiologe. 1976 Jul;16(7):278-82.
3
Achondroplasia: clinical radiologic features with comment on genetic implications.软骨发育不全:临床放射学特征及对遗传学意义的评论
Clin Pediatr (Phila). 1968 Aug;7(8):474-85. doi: 10.1177/000992286800700809.
4
Achondroplasia in two sisters with normal parents.父母正常的两姐妹患软骨发育不全症。
Birth Defects Orig Artic Ser. 1974;10(12):31-6.
5
A glycine 375-to-cysteine substitution in the transmembrane domain of the fibroblast growth factor receptor-3 in a newborn with achondroplasia.一名患有软骨发育不全的新生儿成纤维细胞生长因子受体-3跨膜结构域中发生了甘氨酸375到半胱氨酸的替换。
Eur J Pediatr. 1995 Mar;154(3):215-9. doi: 10.1007/BF01954274.
6
Pseudo-achondrogenesis with fractures.伴有骨折的假性软骨发育不全
Clin Genet. 1972;3(6):435-41. doi: 10.1111/j.1399-0004.1972.tb01477.x.
7
Letter: Failure to diagnose achondroplasia in utero.信件:产前未诊断出软骨发育不全。
Lancet. 1974 Apr 6;1(7858):629. doi: 10.1016/s0140-6736(74)92689-0.
8
Achondroplasia with hypoplastic vertebral bodies secondary to surgical fusion.继发于手术融合的椎体发育不全性软骨发育不全。
Birth Defects Orig Artic Ser. 1974;10(12):356-7.
9
Achondroplasia-hypochondroplasia complex in a newborn infant.一名新生儿的软骨发育不全-软骨发育低下综合征
Am J Med Genet. 1999 Jun 11;84(5):396-400.
10
[Achondroplasia and Down syndrome in the same patient. Report of a case].[同一患者患软骨发育不全和唐氏综合征。病例报告]
Invest Clin. 1999 Jun;40(2):143-54.

引用本文的文献

1
A registry of achondroplasia: a 6-year experience from the Czechia and Slovak Republic.成骨不全症登记处:捷克共和国和斯洛伐克共和国的 6 年经验。
Orphanet J Rare Dis. 2022 Jun 16;17(1):229. doi: 10.1186/s13023-022-02374-x.
2
Birth prevalence of achondroplasia: A systematic literature review and meta-analysis.成骨不全症的出生患病率:系统文献回顾和荟萃分析。
Am J Med Genet A. 2020 Oct;182(10):2297-2316. doi: 10.1002/ajmg.a.61787. Epub 2020 Aug 17.
3
Achondroplasia is defined by recurrent G380R mutations of FGFR3.软骨发育不全由成纤维细胞生长因子受体3(FGFR3)的反复G380R突变所定义。
Am J Hum Genet. 1995 Feb;56(2):368-73.
4
Evidence against the structural gene encoding type II collagen (COL2A1) as the mutant locus in achondroplasia.反对编码II型胶原蛋白(COL2A1)的结构基因作为软骨发育不全突变位点的证据。
J Med Genet. 1986 Feb;23(1):19-22. doi: 10.1136/jmg.23.1.19.
5
The achondroplasia gene is not linked to the locus for neurofibromatosis 1 on chromosome 17.软骨发育不全基因与17号染色体上的神经纤维瘤病1型基因座不连锁。
Hum Genet. 1990 Jun;85(1):12-4. doi: 10.1007/BF00276318.
6
Lethal skeletal dysplasia owing to double heterozygosity for achondroplasia and spondyloepiphyseal dysplasia congenita.由于软骨发育不全和先天性脊柱骨骺发育不良的双重杂合性导致的致死性骨骼发育异常。
J Med Genet. 1992 Nov;29(11):831-3. doi: 10.1136/jmg.29.11.831.