Case report of de novo dup(18p)/del(18q) and r(18) mosaicism.

Gereltzul, Enkhtuvshin; Baba, Yoshiyuki; Suda, Naoto; Shiga, Momotoshi; Inoue, Maristela Sayuri; Tsuji, Michiko; Shin, Insik; Hirata, Yukio; Ohyama, Kimie; Moriyama, Keiji

Gereltzul, Enkhtuvshin; Baba, Yoshiyuki; Suda, Naoto; Shiga, Momotoshi; Inoue, Maristela Sayuri; Tsuji, Michiko; Shin, Insik; Hirata, Yukio; Ohyama, Kimie; Moriyama, Keiji.

Afiliación

Gereltzul E; Maxillofacial Orthognathics, Graduate School, Tokyo Medical and Dental University, 1-5-45, Yushima, Bunkyo-Ku, Tokyo, 113-8549, Japan.
Baba Y; Maxillofacial Orthognathics, Graduate School, Tokyo Medical and Dental University, 1-5-45, Yushima, Bunkyo-Ku, Tokyo, 113-8549, Japan. y-baba.mort@tmd.ac.jp.
Suda N; Maxillofacial Orthognathics, Graduate School, Tokyo Medical and Dental University, 1-5-45, Yushima, Bunkyo-Ku, Tokyo, 113-8549, Japan.
Shiga M; Maxillofacial Orthognathics, Graduate School, Tokyo Medical and Dental University, 1-5-45, Yushima, Bunkyo-Ku, Tokyo, 113-8549, Japan.
Inoue MS; Maxillofacial Orthognathics, Graduate School, Tokyo Medical and Dental University, 1-5-45, Yushima, Bunkyo-Ku, Tokyo, 113-8549, Japan.
Tsuji M; Maxillofacial Orthognathics, Graduate School, Tokyo Medical and Dental University, 1-5-45, Yushima, Bunkyo-Ku, Tokyo, 113-8549, Japan.
Shin I; Maxillofacial Orthognathics, Graduate School, Tokyo Medical and Dental University, 1-5-45, Yushima, Bunkyo-Ku, Tokyo, 113-8549, Japan.
Hirata Y; Clinical and Molecular Endocrinology, Graduate School, Tokyo Medical and Dental University, Tokyo, Japan.
Ohyama K; Maxillofacial Orthognathics, Graduate School, Tokyo Medical and Dental University, 1-5-45, Yushima, Bunkyo-Ku, Tokyo, 113-8549, Japan.
Moriyama K; Maxillofacial Orthognathics, Graduate School, Tokyo Medical and Dental University, 1-5-45, Yushima, Bunkyo-Ku, Tokyo, 113-8549, Japan.

J Hum Genet ; 53(10): 941-946, 2008.

Article en En | MEDLINE | ID: mdl-18679767

Asunto(s)

Aberraciones Cromosómicas; Cromosomas Humanos Par 18/genética; Hipogonadismo/genética; Hipotiroidismo/genética; Mosaicismo; Adulto; Bandeo Cromosómico; Femenino; Humanos; Hibridación Fluorescente in Situ

Texto completo

Añadir a Mi BVS

Imprimir

XML

PubMed Links

Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Cromosomas Humanos Par 18 / Aberraciones Cromosómicas / Hipogonadismo / Hipotiroidismo / Mosaicismo Tipo de estudio: Prognostic_studies Límite: Adult / Female / Humans Idioma: En Revista: J Hum Genet Asunto de la revista: GENETICA MEDICA Año: 2008 Tipo del documento: Article País de afiliación: Japón Pais de publicación: Reino Unido

Texto completo

Añadir a Mi BVS

Imprimir

XML

PubMed Links

Buscar en Google