[因遗传性易位t(1;10)(q44;q22)导致的10号染色体部分三体] - Suppr

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[Partial trisomy 10 due to hereditary translocation t(1;10)(q44;q22)].

作者信息

Laurent C, Bovier-Lapierre M, Dutrillaux B

出版信息

Humangenetik. 1973;18(4):321-7. doi: 10.1007/BF00291129.

DOI:10.1007/BF00291129

PMID:4200006

Abstract

摘要

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本文引用的文献

MEIOTIC AND MITOTIC STUDIES OF A FAMILIAL RECIPROCAL TRANSLOCATION BETWEEN TWO AUTOSOMES OF GROUP 6-12.

Cytogenetics. 1965;4:45-64. doi: 10.1159/000129843.

Familial reciprocal C/18 translocation.

Am J Hum Genet. 1966 Nov;18(6):572-83.

A translocation t (Bq+: Cq-) in a West Indian family and a report of a second family showing a possible long arm group B translocation.

Arch Dis Child. 1969 Feb;44(233):106-12. doi: 10.1136/adc.44.233.106.

New translocation in three generations of a family.

J Med Genet. 1968 Sep;5(3):200-4. doi: 10.1136/jmg.5.3.200.

[Multiple malformations in partial trisomy C (12) as manifestation of an inherited E-C (18/12) translocation].

Helv Paediatr Acta. 1967 Apr;22(1):41-53.

[Partial trisomy C by t(Cq-; Dp+) translocation with a C(p- q+) remnant].

Arch Fr Pediatr. 1967 Oct;24(8):859-68.

Analysis of human metaphase chromosome set by aid of DNA-binding fluorescent agents.

Exp Cell Res. 1970 Oct;62(2):490-2. doi: 10.1016/0014-4827(70)90586-0.

[Partial trisomy C through a familial translocation t(Cq+;Cq-)].

Ann Genet. 1968 Sep;11(3):171-5.

[6-12 13-15 translocation and partial 6-12 trisomy (probably 10)].

Ann Genet. 1965;8(1):16-20.

[Clinical and cytogenetic observations on 2 mosaic C trisomic adults. Individualization of the supernumerary chromosome with the modern denaturation technic: 47, XY, ?8 +].

Lyon Med. 1971 Dec 26;226(20):827-33.

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