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...

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Detalhes bibliográficos
Main Authors: 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
Formato: Artigo
Idioma:Inglês
Publicado em: Cold Spring Harbor Laboratory Press 1999
Assuntos:
Letter
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC310730/
https://ncbi.nlm.nih.gov/pubmed/10077533
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