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Am J Hum Genet. 1976 Jul;28(4):400-3.
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Individuals with nonsyndromic orofacial clefts have increased asymmetry of fingerprint patterns.非综合征性口面裂个体的指纹模式存在不对称性增加。
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Dermatoglyphic Analysis in Parents with Cleft Children: A Comparative Study.患有唇腭裂患儿的父母的皮纹分析:一项对比研究。
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Can Dermatoglyphics Be Used as a Marker for Predicting Future Malocclusions?皮纹学能否作为预测未来错牙合畸形的标志物?
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8
Human handedness and the concept of developmental stability.
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9
A study of fluctuating dermatoglyphic asymmetry in the sibs and parents of cleft lip propositi.唇腭裂患者同胞及父母指纹波动不对称性的研究
Am J Hum Genet. 1977 Sep;29(5):503-7.
10
Cleft lip and dermatoglyphic asymmetry.唇裂与皮纹不对称。
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本文引用的文献

1
Trisomy 13-15: a clinical syndrome.13 - 15三体综合征:一种临床综合征。
Lancet. 1961 Nov 4;2(7210):1001-2. doi: 10.1016/s0140-6736(61)90963-1.
2
A genetic study of cleft lip and palate in Utah.犹他州唇腭裂的遗传学研究。
Am J Hum Genet. 1963 Jun;15(2):209-15.
3
A study of major congenital defects in Japanese infants.一项关于日本婴儿主要先天性缺陷的研究。
Am J Hum Genet. 1958 Dec;10(4):398-445.
4
Fistula labii inferioris congenita and its association with cleft lip and palate.先天性下唇瘘及其与唇腭裂的关联。
Am J Hum Genet. 1954 Jun;6(2):244-56.
5
Genetics of common disorders.常见疾病的遗传学
Br Med Bull. 1969 Jan;25(1):52-7. doi: 10.1093/oxfordjournals.bmb.a070671.
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Developmental 'noise' and a congenital malformation.发育“噪音”与先天性畸形
Genet Res. 1967 Dec;10(3):313-7. doi: 10.1017/s0016672300011071.
7
Cleft lip and palate in parent and child.父母与子女患唇腭裂。
Plast Reconstr Surg. 1969 Nov;44(5):436-40.
8
Congenital cleft lip. A genetic study of 496 propositi.先天性唇裂。对496名先证者的遗传学研究。
J Med Genet. 1971 Mar;8(1):65-83. doi: 10.1136/jmg.8.1.65.
9
Technique for recording dermatoglyphics.皮纹记录技术。
Lancet. 1971 Feb 27;1(7696):432-3. doi: 10.1016/s0140-6736(71)92417-2.

先天性唇裂与波动性皮纹不对称。

Congenital cleft lip and fluctuating dermatoglyphic asymmetry.

作者信息

Woolf C M, Gianas A D

出版信息

Am J Hum Genet. 1976 Jul;28(4):400-3.

PMID:941907
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1685050/
Abstract

Fluctuating asymmetry for the palmar atd angle was studied in propositi born with CL(P) and their normal parents and sibs. The propositi with a family history of this congenital malformation were significantly different from the controls for this type of asymmetry. The propositi without a family history and the normal parents and sibs of both types of propositi were similar to the controls. The difference between the two types of propositi suggests that in some individuals a genetic mechanism may account for CL(P) and increased fluctuating asymmetry for this dermatoglyphic trait.

摘要

对患有先天性唇腭裂(CL(P))的研究对象及其正常父母和兄弟姐妹的手掌atd角的波动不对称性进行了研究。有这种先天性畸形家族史的研究对象在这种不对称类型上与对照组有显著差异。没有家族史的研究对象以及两类研究对象的正常父母和兄弟姐妹与对照组相似。两类研究对象之间的差异表明,在某些个体中,一种遗传机制可能导致先天性唇腭裂(CL(P))以及这种皮纹特征的波动不对称性增加。