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9号染色体短臂三体的一例新病例。

A new case of trisomy for the short arm of No. 9 chromosome.

作者信息

Baccichetti C, Tenconi R

出版信息

J Med Genet. 1973 Sep;10(3):296-9. doi: 10.1136/jmg.10.3.296.

Abstract

A new case with trisomy for the short arm of No. 9 chromosome, identified by heat treatment and Giemsa staining is reported. The clinical picture and dermatoglyphic patterns are similar to those previously reported.

摘要

报告了1例经热处理和吉姆萨染色鉴定的9号染色体短臂三体新病例。临床表现和皮纹模式与先前报道的相似。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3432/1013037/419b38b36a5f/jmedgene00324-0097-a.jpg

引用本文的文献

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Chromosome 15 anomalies and the Prader-Willi syndrome: cytogenetic analysis.
Hum Genet. 1984;66(4):313-34. doi: 10.1007/BF00287636.
3
A case of partial (9p) trisomy in a family with a balanced translocation 46,XX,t(1p+9q-).
J Med Genet. 1975 Sep;12(3):310-4. doi: 10.1136/jmg.12.3.310.
4
Partial 9 trisomy by 3:1 segregation of balanced maternal translocation (7q+; 9q-).
J Med Genet. 1975 Sep;12(3):301-5. doi: 10.1136/jmg.12.3.301.
5
A case of trisomy 9p in a family with translocation 9/15.
Humangenetik. 1975;27(4):353-8. doi: 10.1007/BF00278432.
6
Possible intrachromosomal duplication in a case of trisomy 9p.
Hum Genet. 1976 Oct 28;34(2):217-21. doi: 10.1007/BF00278892.
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A case of trisomy for the short arm of chromosome no. 9(+9(p)).
Hum Genet. 1976 Sep 10;34(1):77-80. doi: 10.1007/BF00284440.
8
47,+(9q-) in unrelated three children with plasma growth hormone deficiency.
Hum Genet. 1976 Mar 12;31(3):271-82. doi: 10.1007/BF00270857.
9
Trisomy 9p resulting from maternal 9/21 translocation.
Hum Genet. 1976 May 19;32(2):217-20. doi: 10.1007/BF00291508.
10
Pure partial trisomy for long arm of chromosome 9.
J Med Genet. 1976 Jun;13(3):239-42. doi: 10.1136/jmg.13.3.239.

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