10号染色体短臂缺失。 - Suppr

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Deletion of the short arm of chromosome No. 10.

作者信息

Berger R, Larroche J C, Toubas P L

出版信息

Acta Paediatr Scand. 1977 Sep;66(5):659-62. doi: 10.1111/j.1651-2227.1977.tb07965.x.

DOI:10.1111/j.1651-2227.1977.tb07965.x

PMID:899785

Abstract

摘要

相似文献

Deletion of the short arm of chromosome No. 10.10号染色体短臂缺失。

Acta Paediatr Scand. 1977 Sep;66(5):659-62. doi: 10.1111/j.1651-2227.1977.tb07965.x.

A partial long arm deletion of chromosome 7:46,XY,del(7)(q32).7号染色体长臂部分缺失：46，XY，del(7)(q32)

J Med Genet. 1977 Apr;14(2):144-7. doi: 10.1136/jmg.14.2.144.

[9p syndrome. Deletion of the short arm of chromosome 9; Monosomy of short arm 9].[9p综合征。9号染色体短臂缺失；9号染色体短臂单体性]

Ugeskr Laeger. 1977 Jan;139(4):204.

[Interstitial deletion of the long arm of chromosome 7 in a female child with leprechaunism].[一名患矮妖精貌综合征女童的7号染色体长臂间质性缺失]

Ann Genet. 1976 Dec;19(4):265-8.

Interstitial deletion of the long arm of chromosome no. 7 (7q-) in an infant with multiple anomalies.一名患有多种异常的婴儿出现7号染色体长臂间质性缺失（7q-）。

Clin Genet. 1976 Nov;10(5):307-12. doi: 10.1111/j.1399-0004.1976.tb00053.x.

[Partial deletion of the short arm of the chromosome 9].[9号染色体短臂部分缺失]

Ann Genet. 1976 Jun;19(2):143.

Partial deletion of the short arm of chromosome 12(p11; p13). Report of a case.12号染色体短臂部分缺失（p11；p13）。病例报告。

Ann Genet. 1975 Jun;18(2):95-8.

9pter leads p22 deletion syndrome: a case report.9号染色体短臂末端至p22缺失综合征：一例报告

Birth Defects Orig Artic Ser. 1976;12(5):151-5.

Interstitial deletion of the long arm of chromosome 2 in a malformed infant with karyotype 46,XX,del(2)(q31q33).一名核型为46,XX,del(2)(q31q33)的畸形婴儿存在2号染色体长臂的间质缺失。

Am J Med Genet. 1986 Nov;25(3):405-11. doi: 10.1002/ajmg.1320250302.

Deletion in the short arm of chromosome 9 from a subject with congenital cerebral maldevelopment. Repository identification No. GM-870.一名患有先天性脑发育不良患者的9号染色体短臂缺失。储存库识别号GM - 870。

Cytogenet Cell Genet. 1976;17(5):296-7. doi: 10.1159/000130726.

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Clinical report of a neonate carrying a large deletion in the 10p15.3p13 region and review of the literature.一名携带10p15.3p13区域大片段缺失的新生儿临床报告及文献复习

Mol Cytogenet. 2021 May 28;14(1):29. doi: 10.1186/s13039-021-00546-1.

Immunodeficiency in DiGeorge Syndrome and Options for Treating Cases with Complete Athymia.DiGeorge综合征中的免疫缺陷及完全无胸腺病例的治疗选择

Front Immunol. 2013 Oct 31;4:322. doi: 10.3389/fimmu.2013.00322.

MRI findings in a patient with partial monosomy 10p.一名患有10p部分单体综合征患者的磁共振成像（MRI）检查结果

J Med Genet. 1998 Feb;35(2):159-61. doi: 10.1136/jmg.35.2.159.

Partial monosomy 10p syndrome.10p部分单体综合征

Eur J Pediatr. 1981 Oct;137(2):243-6. doi: 10.1007/BF00441326.

Two chromosomal syndromes in the same family: monosomy and trisomy for part of the short arm of chromosome 10.同一家族中的两种染色体综合征：10号染色体短臂部分单体性和三体性。

Eur J Pediatr. 1982 Oct;139(2):153-7. doi: 10.1007/BF00441502.

Partial monosomy of chromosome 10 short arms.10号染色体短臂部分单体性

J Med Genet. 1983 Apr;20(2):107-11. doi: 10.1136/jmg.20.2.107.

Renal and urinary tract abnormalities associated with chromosome aberrations.与染色体畸变相关的肾脏和泌尿道异常。

Int J Pediatr Nephrol. 1987 Oct-Dec;8(4):215-26.

10p- syndrome associated with multiple chromosomal abnormalities.与多种染色体异常相关的10p-综合征

Hum Genet. 1978 Dec 18;45(2):229-35. doi: 10.1007/BF00286969.

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