Delineation of trisomy 9 syndrome.
作者信息
Romain D R, Sullivan J
出版信息
J Med Genet. 1983 Apr;20(2):156-7. doi: 10.1136/jmg.20.2.156.
Abstract
摘要
相似文献
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Delineation of trisomy 9 syndrome.9号染色体三体综合征的描述。
J Med Genet. 1983 Apr;20(2):156-7. doi: 10.1136/jmg.20.2.156.
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[Trisomy 9p - clinical and cytogenetic syndrome].9号染色体短臂三体综合征 - 临床与细胞遗传学综合征
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[Trisomy 10p as a result of familial 10/22 translocation].[由于家族性10/22易位导致的10号染色体短臂三体]
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Syndromes due to chromosomal abnormalities: partial trisomy 22, interstitial deletion of the long arm of 13, and trisomy 8.
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Partial trisomy 9q-in a polymalformed new-born infant. Karyotype: 47,XX, + del (9) (q33).9q部分三体综合征——见于一名多发畸形的新生儿。核型：47,XX, + del(9)(q33) 。
Acta Paediatr Belg. 1978 Oct-Dec;31(4):237-40.
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Case report: A case report and literature review of complete trisomy 9.病例报告：9号染色体完全三体的病例报告及文献综述
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Gene-rich chromosome regions and autosomal trisomy. A case of chromosome 3 trisomy mosaicism.基因丰富的染色体区域与常染色体三体性。一例3号染色体三体性嵌合体病例。
Hum Genet. 1987 Nov;77(3):214-20. doi: 10.1007/BF00284472.
本文引用的文献
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Extra band in the 9qh+ chromosome in a normal father and in his child with multiple congenital anomalies.一名正常父亲及其患有多种先天性异常的孩子的9qh+染色体出现额外条带。
Hum Genet. 1982;60(3):294. doi: 10.1007/BF00303025.
2
Prenatal diagnosis of trisomy 9.9三体综合征的产前诊断
Humangenetik. 1975 Sep 23;29(3):243-50. doi: 10.1007/BF00297630.
3
Trisomy 9 associated with an enlarged 9qh segment in a liveborn.
Hum Genet. 1976 Dec 15;34(3):323-5. doi: 10.1007/BF00295299.
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An extra band in human 9qh+ chromosomes.人类9号染色体长臂增加的一条带。
Hum Genet. 1978 Sep 19;43(3):259-64. doi: 10.1007/BF00278832.
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