DUPLICATION OF THE SHORT ARM OF THE X-CHROMOSOME IN MOTHER AND DAUGHTER


Autoria(s): Tuckmuller, C. M.; Martinez, J. E.; Batista, DAS; Kearns, W. G.; Wertelecki, W.
Contribuinte(s)

Universidade Estadual Paulista (UNESP)

Data(s)

20/05/2014

20/05/2014

01/05/1993

Resumo

An 11-year-old girl with short stature, mental retardation, and mild dysmorphic features was found to have an inverted duplication of most of the short arm of the X chromosome [dic inv dup(X)(qter --> p22.3 = p22.3 --> cen:)]. Her mother, who is also short and retarded, carries the same duplication. Fluorescence in situ hybridization with an X chromosome library, and with X centromere-specific alpha satellite and telomere probes, was useful in characterizing the duplication. In most females with structurally abnormal X chromosomes, the abnormal chromosome is inactivated. Although the duplicated X was consistently late replicating in the mother, X chromosome inactivation studies in the proband indicated that in 11 % of her lymphocytes the duplicated X was active.

Formato

395-400

Identificador

http://dx.doi.org/10.1007/BF00217366

Human Genetics. New York: Springer Verlag, v. 91, n. 4, p. 395-400, 1993.

0340-6717

http://hdl.handle.net/11449/36654

10.1007/BF00217366

WOS:A1993LF65900021

Idioma(s)

eng

Publicador

Springer

Relação

Human Genetics

Direitos

closedAccess

Tipo

info:eu-repo/semantics/article