QR-Code

High-Resolution Physical and Genetic Mapping of the Critical Region for Meckel Syndrome and Mulibrey Nanism on Chromosome 17q22–q23

Previously, we assigned the genes for two autosomal recessive disorders, Meckel syndrome (MKS; MIM 249000) and Mulibrey Nanism [MUL (muscle–liver–brain–eye Nanism); MIM 253250] that are enriched in the Finnish population, to overlapping genomic regions on chromosome 17q. Now, we report the construct...

Ausführliche Beschreibung

Gespeichert in:
Veröffentlicht in:Genome Res
Hauptverfasser: Paavola, Paulina, Avela, Kristiina, Horelli-Kuitunen, Nina, Bärlund, Maarit, Kallioniemi, Anne, Idänheimo, Niina, Kyttälä, Mira, de la Chapelle, Albert, Palotie, Aarno, Lehesjoki, Anna-Elina, Peltonen, Leena
Format: Artigo
Sprache:Inglês
Veröffentlicht: Cold Spring Harbor Laboratory Press 1999
Schlagworte:
Letter
Online-Zugang:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC310730/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/10077533/
Tags: Tag hinzufügen
Keine Tags, Fügen Sie das erste Tag hinzu!

Ähnliche Einträge