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Sex chromosomal abnormalities (SCA): a prospective and longitudinal study of newborns identified in an unbiased manner.

作者信息

Robinson A, Bender B, Borelli J, Puck M, Salbenblatt J, Webber M L

出版信息

Birth Defects Orig Artic Ser. 1982;18(4):7-39.

PMID:7159724
Abstract
摘要

相似文献

1
Sex chromosomal abnormalities (SCA): a prospective and longitudinal study of newborns identified in an unbiased manner.性染色体异常（SCA）：一项对以无偏倚方式识别出的新生儿进行的前瞻性纵向研究。
Birth Defects Orig Artic Ser. 1982;18(4):7-39.
2
Growth and development of children with X and Y chromosome aneuploidy from infancy to pubertal age: the Toronto study.
Birth Defects Orig Artic Ser. 1982;18(4):99-154.
3
Studies on infants and children with sex chromosomal abnormalities.对患有性染色体异常的婴幼儿及儿童的研究。
Adv Pathobiol. 1977(6):214-26.
4
Follow-up until age 7 to 11 of 25 unselected children with sex chromosome abnormalities.对25名未经挑选的性染色体异常儿童进行随访至7至11岁。
Birth Defects Orig Artic Ser. 1982;18(4):61-97.
5
The Edinburgh study of growth and development of children with sex chromosome abnormalities.
Birth Defects Orig Artic Ser. 1982;18(4):41-60.
6
Summary of clinical findings of children with 47,XXY, 47,XYY, and 47,XXX karyotypes.47,XXY、47,XYY和47,XXX核型患儿的临床检查结果总结。
Birth Defects Orig Artic Ser. 1982;18(4):1-5.
7
Sex chromosomal aneuploidy: prospective and longitudinal studies.
Birth Defects Orig Artic Ser. 1986;22(3):23-71.
8
Sex chromosome aneuploidy: the Denver Prospective Study.性染色体非整倍体：丹佛前瞻性研究
Birth Defects Orig Artic Ser. 1990;26(4):59-115.
9
A prospective study of development of children with sex chromosome anomalies - New Haven study III. The middle years.
Birth Defects Orig Artic Ser. 1982;18(4):193-218.
10
[Early recognition and diagnosis of X-chromosome abnormalities in phenotypically female individuals in childhood].[儿童期表型为女性个体中X染色体异常的早期识别与诊断]
Wien Med Wochenschr. 1970 May 16;120(20):362-5.

引用本文的文献

1
Neurodevelopmental and Mental Health Outcomes in a National Clinical Sample of Youth With Sex Chromosome Trisomies Compared With Matched Controls.与匹配对照组相比，全国性青年性染色体三体临床样本中的神经发育和心理健康结果。
J Dev Behav Pediatr. 2025;46(2):e208-e215. doi: 10.1097/DBP.0000000000001342. Epub 2025 Jan 9.
2
Supporting students with sex chromosome aneuploidies in educational settings: Results of a nationwide survey.支持性染色体非整倍体学生在教育环境中的发展：全国性调查的结果。
J Sch Psychol. 2022 Aug;93:28-40. doi: 10.1016/j.jsp.2022.06.002. Epub 2022 Jun 28.
3
Early neurodevelopmental and medical profile in children with sex chromosome trisomies: Background for the prospective eXtraordinarY babies study to identify early risk factors and targets for intervention.
性染色体三体患儿的早期神经发育和医学特征：开展前瞻性 eXtraordinarY babies 研究以识别早期风险因素和干预靶点的背景。
Am J Med Genet C Semin Med Genet. 2020 Jun;184(2):428-443. doi: 10.1002/ajmg.c.31807. Epub 2020 Jun 7.
4
Triple X syndrome: a review of the literature.三 X 综合征：文献回顾。
Eur J Hum Genet. 2010 Mar;18(3):265-71. doi: 10.1038/ejhg.2009.109. Epub 2009 Jul 1.
5
Sex chromosomal anomalies: prospective studies in children.
Behav Genet. 1983 Jul;13(4):321-9. doi: 10.1007/BF01065770.
6
The meaning of early knowledge of a child's infertility in families with 47,XXY and 45,X children.患有47,XXY和45,X染色体疾病儿童的家庭中，早期知晓孩子不育症的意义。
Child Psychiatry Hum Dev. 1984 Summer;14(4):215-22. doi: 10.1007/BF00706035.
7
Dyslexia in 47,XXY boys identified at birth.出生时确诊的47，XXY男孩的阅读障碍。
Behav Genet. 1986 May;16(3):343-54. doi: 10.1007/BF01071315.
8
An XXX male resulting from paternal X-Y interchange and maternal X-X nondisjunction.一名由父源X-Y易位和母源X-X不分离导致的XXX男性。
Am J Hum Genet. 1987 Oct;41(4):594-604.