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DiGeorge syndrome: an historical review of clinical and cytogenetic features.

作者信息

Greenberg F

机构信息

Institute for Molecular Genetics, Baylor College of Medicine, Houston, Texas.

出版信息

J Med Genet. 1993 Oct;30(10):803-6. doi: 10.1136/jmg.30.10.803.

Abstract
摘要

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本文引用的文献

1
Congenital absence of the parathyroid glands.
AMA Arch Pathol. 1959 Apr;67(4):412-5.
2
Velo-cardio-facial syndrome: a review of 120 patients.
Am J Med Genet. 1993 Feb 1;45(3):313-9. doi: 10.1002/ajmg.1320450307.
4
Spectrum of the DiGeorge "syndrome".
J Pediatr. 1980 May;96(5):955-6. doi: 10.1016/s0022-3476(80)80599-3.
5
A deletion in chromosome 22 can cause DiGeorge syndrome.
Hum Genet. 1981;57(3):253-6. doi: 10.1007/BF00278938.
6
The association of the DiGeorge anomalad with partial monosomy of chromosome 22.
J Pediatr. 1982 Aug;101(2):197-200. doi: 10.1016/s0022-3476(82)80116-9.
7
Familial DiGeorge syndrome and associated partial monosomy of chromosome 22.
Hum Genet. 1984;65(4):317-9. doi: 10.1007/BF00291554.
9
DiGeorge syndrome(s).
J Pediatr. 1972 Nov;81(5):1042-4. doi: 10.1016/s0022-3476(72)80575-4.
10

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