Saltar ao contenido
VuFind
    • English
    • Deutsch
    • Español
    • Français
    • Italiano
    • 日本語
    • Nederlands
    • Português
    • Português (Brasil)
    • 中文(简体)
    • 中文(繁體)
    • Türkçe
    • עברית
    • Gaeilge
    • Cymraeg
    • Ελληνικά
    • Català
    • Euskara
    • Русский
    • Čeština
    • Suomi
    • Svenska
    • polski
    • Dansk
    • slovenščina
    • اللغة العربية
    • বাংলা
    • Galego
    • Tiếng Việt
    • Hrvatski
    • हिंदी
    • Հայերէն
    • Українська
    • Sámegiella
    • Монгол
Avanzado
  • Assignment of the human RhoHP1...
  • Citar
  • Text this
  • Enviar este rexistro por email
  • Imprimir
  • Exportar rexistro
    • Exportar a RefWorks
    • Exportar a EndNoteWeb
    • Exportar a EndNote
  • Permanent link
Assignment of the human RhoHP1 gene (ARHD) to chromosome 11q14.3 by radiation hybrid mapping.

Assignment of the human RhoHP1 gene (ARHD) to chromosome 11q14.3 by radiation hybrid mapping.

Detalles Bibliográficos
Main Authors: Kim, H, Choi, J, Jung, A, Jang, K, Lee, W, Choi, W, Crow, T, Hyun, B
Formato: Journal article
Idioma:English
Publicado: 2000
  • Existencias
  • Descripción
  • Títulos similares
  • Staff View

Títulos similares

  • Assignment of the endogenous retrovirus HERV-R (ERV3) to human chromosome 7q11.2 by radiation hybrid mapping.
    por: Kim, H, et al.
    Publicado: (2000)
  • Tetrasomy of 11q13.4-q14.3 due to an intrachromosomal triplication associated with paternal uniparental isodisomy for 11q14.3-qter, intrauterine growth restriction, developmental delay, corpus callosum dysgenesis, microcephaly, congenital heart defects and facial dysmorphism
    por: Chih-Ping Chen, et al.
    Publicado: (2021-01-01)
  • Isolation of new probes in the region of the Wilson disease locus, 13q14.2-->q14.3.
    por: Bull, P, et al.
    Publicado: (1993)
  • Detection of chromosome 5q interstitial deletion of 5q14.3-q31.1 by chromosome microarray analysis in a second-trimester fetus with multiple congenital anomalies and a literature review of chromosome 5q interstitial deletion syndrome
    por: Chih-Ping Chen, et al.
    Publicado: (2024-11-01)
  • PHYSICAL MAPPING OF 13Q14.3 FOCUSED ON THE REGION OF THE WILSON DISEASE LOCUS
    por: Bull, P, et al.
    Publicado: (1993)

Opciones de procura

  • Historial de Procuras
  • Procura avanzada

Buscar Máis

  • Revisar o catálogo
  • Lista alfabética
  • Explore Channels
  • Reservas de curso
  • Novos exemplares

Necesita Axuda?

  • Consello de procura
  • Consulte a un Bibliotecario
  • Preguntas Frecuentes