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Apparent G-monosomy, G-deletion, and incomplete Down's syndrome in a single family.

作者信息

Schmidt R, Mundel G, Rosenblatt M, Katznelson M B

出版信息

J Med Genet. 1972 Dec;9(4):457-61. doi: 10.1136/jmg.9.4.457.

Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd7f/1469069/2a6c8861a3c0/jmedgene00363-0075-a.jpg

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本文引用的文献

1
Apparent monosomy of a G autosome in a Jamaican infant.
J Med Genet. 1966 Dec;3(4):290-2. doi: 10.1136/jmg.3.4.290.
2
[PARTIAL MONOSOMY FOR A SMALL ACROCENTRIC CHROMOSOME].
C R Hebd Seances Acad Sci. 1964 Nov 30;259:4187-90.
3
The use of dermal configurations in the diagnosis of mongolism.
J Pediatr. 1957 Jan;50(1):19-26. doi: 10.1016/s0022-3476(57)80005-5.
4
Autosomal monosomy in man. Complete monosomy G (21-22) in a four-and-one-half-year-old mentally retarded girl.
N Engl J Med. 1967 Oct 12;277(15):777-84. doi: 10.1056/NEJM196710122771502.
5
A child with partial deletion of a G-group autosome.
Am J Dis Child. 1967 Sep;114(3):336-9. doi: 10.1001/archpedi.1967.02090240150018.
7
A patient with 45,XX,Gminus-46,XX,Gr mosaicism.
J Med Genet. 1969 Jun;6(2):220-3. doi: 10.1136/jmg.6.2.220.
8
Monosomy for a G autosome.
Arch Dis Child. 1969 Feb;44(233):113-9. doi: 10.1136/adc.44.233.113.
10
The G deletion syndromes.
J Pediatr. 1970 Oct;77(4):658-63. doi: 10.1016/s0022-3476(70)80209-8.

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