4号染色体短臂部分缺失（4p-）：5例非亲缘关系患者的临床研究 - Suppr

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超能文献

Partial deletion of the short arm of chromosome no. 4(4p-): clinical studies in five unrelated patients.

作者信息

Miller O J, Breg W R, Warburton D, Miller D A, DeCapoa A, Allderdice P W, Davis J, Klinger H P, McGilvray E, Allen F H

出版信息

J Pediatr. 1970 Nov;77(5):792-801. doi: 10.1016/s0022-3476(70)80237-2.

DOI:10.1016/s0022-3476(70)80237-2

PMID:5504070

Abstract

摘要

相似文献

Partial deletion of the short arm of chromosome no. 4(4p-): clinical studies in five unrelated patients.4号染色体短臂部分缺失（4p-）：5例非亲缘关系患者的临床研究

J Pediatr. 1970 Nov;77(5):792-801. doi: 10.1016/s0022-3476(70)80237-2.

Partial deletion of the short arm of a chromosome No. 4. Wolf's syndrome.4号染色体短臂部分缺失。沃尔夫综合征。

Maandschr Kindergeneeskd. 1967 Oct;35(8):252-69.

Cri-du-chat syndrome. Case report.猫叫综合征。病例报告。

Helv Paediatr Acta. 1967 Apr;22(1):22-7.

[Partial deletion of the short arm of chromosome 4 (Wolf's syndrome). Two further cases].[4号染色体短臂部分缺失（沃尔夫综合征）。另外两例]

Arch Genet (Zur). 1972;45(2):88-98.

Translocation 4p-- syndrome: a general review.4p-综合征：综述

Am J Dis Child. 1975 Mar;129(3):366-70. doi: 10.1001/archpedi.1975.02120400066017.

[Deficiency in the short arms of Group B (4p--; 5p--) chromosomes. Studies on 6 patients].[B组染色体短臂缺失（4p--；5p--）。对6例患者的研究]

Z Kinderheilkd. 1971;110(3):218-47.

Partial deletion of short arm of chromosome no. 4.

J Pediatr. 1971 May;78(5):911-2. doi: 10.1016/s0022-3476(71)80378-5.

The "cri du chat" syndrome.“猫叫综合征”。

Sov Genet. 1970 Oct;6(10):1374-9.

B group short-arm deletion syndrome.

Birth Defects Orig Artic Ser. 1971 Jun;7(7):89-97.

[Clinical and cytogenetic differential diagnosis of the anomalies of the short arms of the B chromosomes].[B染色体短臂异常的临床与细胞遗传学鉴别诊断]

Z Kinderheilkd. 1967;98(3):235-45.

引用本文的文献

Oral Manifestations of Wolf-Hirschhorn Syndrome: Genotype-Phenotype Correlation Analysis.沃尔夫-赫希霍恩综合征的口腔表现：基因型-表型相关性分析。

J Clin Med. 2020 Nov 4;9(11):3556. doi: 10.3390/jcm9113556.

Neuropathological findings in Wolf-Hirschhorn (4p-) syndrome.

Acta Neuropathol. 1981;55(2):163-5. doi: 10.1007/BF00699242.

Familial centric fission of chromosome 4.4号染色体的家族性中心粒分裂

J Med Genet. 1984 Oct;21(5):388-91. doi: 10.1136/jmg.21.5.388.

A ring-4 chromosome in a patient with normal intelligence and short stature.一名智力正常但身材矮小患者的4号环状染色体。

J Med Genet. 1971 Dec;8(4):517-21. doi: 10.1136/jmg.8.4.517.

The 4p-syndrome, with a report of two new cases.

Humangenetik. 1973;19(1):99-109. doi: 10.1007/BF00295238.

Further observations on a previously reported case of 4p--syndrome.

Humangenetik. 1972;15(4):361-3. doi: 10.1007/BF00281740.

Malformations of kidney and urinary tract in common chromosomal aberrations. II. Morphogenetic studies.常见染色体畸变中的肾和尿路畸形。II. 形态发生学研究。

Humangenetik. 1973 Mar 23;18(1):16-32. doi: 10.1007/BF00279027.

A pericentric inversion of a chromosome 4 with a t(4q+10p-) and a familial t(DqDq) in a mentally retarded girl.一名智力发育迟缓女孩存在4号染色体的臂间倒位，伴有t(4q+10p-)以及家族性t(DqDq)。

Humangenetik. 1974;25(1):69-78. doi: 10.1007/BF00281009.

Chromosome 3 duplication q21 leads to qter deletion p25 leads to pter syndrome in children of carriers of a pericentric inversion inv(3) (p25q21).3号染色体q21重复导致qter缺失，p25导致pter综合征，见于臂间倒位inv(3)(p25q21)携带者的子女。

Am J Hum Genet. 1975 Nov;27(6):699-718.

The 8p- syndrome.8号染色体短臂缺失综合征

Hum Genet. 1979 Mar 12;47(2):135-40. doi: 10.1007/BF00273195.

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