相似文献
1
[Ring chromosomes in mosaicism 46, XY, Cr-46, XY].
Arch Genet (Zur). 1973;46(1):1-14.
2
Structural variation in human nitotic chromosomes.
Ann Acad Sci Fenn Biol. 1971;179:1-69.
3
[Study by fluorescence of a trisomy C mosaic, probably 8: 46,XY-47,XY,?8+].
Ann Genet. 1971 Mar;14(1):69-72.
4
46,XY-47,XY,C+ mosaicism in a male infant with multiple anomalies.
Ann Genet. 1969 Jun;12(2):102-6.
5
6
[C-G translocation: karyotype 46, XY,t(Cq-; Gq+): parents 46, XX and 46, XY].
Acta Paediatr Belg. 1971;25(2):119-26.
7
[4 cases of trisomy for the short arm of chromosome 9. Individualization of a new morbid entity].
Ann Genet. 1970 Dec;13(4):217-32.
8
Familial translocation between chromosomes of groups C and D (46, T(Cq-;Dq+).
Sov Genet. 1974 Jun 1;8(5):651-7.
9
[46,XY-45,X mosaicism and 18p- deletion].
Ann Genet. 1971 Mar;14(1):59-62.
10
Duplication 11 (q21 to 23 leads to qter) syndrome.
Birth Defects Orig Artic Ser. 1977;13(3B):167-86.
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