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...

全面介紹

Na minha lista:
書目詳細資料
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
格式: Artigo
語言:Inglês
出版: Cold Spring Harbor Laboratory Press 1999
主題:
Letter
在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC310730/
https://ncbi.nlm.nih.gov/pubmed/10077533
標簽: 添加標簽
沒有標簽, 成為第一個標記此記錄!

相似書籍