A physical map of the mouse shaker-2 region contains many of the genes commonly deleted in Smith-Magenis syndrome (del17p11.2p11.2).

scientific article published in February 1999

A physical map of the mouse shaker-2 region contains many of the genes commonly deleted in Smith-Magenis syndrome (del17p11.2p11.2). is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1006/GENO.1998.5669
P698PubMed publication ID10049592

P50authorSally A. CamperQ40082925
P2093author name stringZhao Q
Wang A
Friedman TB
Chen KS
Lupski JR
Probst FJ
P433issue3
P921main subjectSmith-Magenis syndromeQ2295338
P304page(s)348-352
P577publication date1999-02-01
P1433published inGenomicsQ5533503
P1476titleA physical map of the mouse shaker-2 region contains many of the genes commonly deleted in Smith-Magenis syndrome (del17p11.2p11.2).
P478volume55

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cites work (P2860)
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Q24537317Fliih, a gelsolin-related cytoskeletal regulator essential for early mammalian embryonic development
Q47844365Fliih, the murine homologue of the Drosophila melanogaster flightless I gene: nucleotide sequence, chromosomal mapping and overlap with Llglh
Q24672496Genes in a refined Smith-Magenis syndrome critical deletion interval on chromosome 17p11.2 and the syntenic region of the mouse
Q37198442Genomic disorders ten years on.
Q35550640Human Nonsyndromic Sensorineural Deafness
Q34699430Molecular-evolutionary mechanisms for genomic disorders
Q28590294Mouse cytosolic and mitochondrial deoxyribonucleotidases: cDNA cloning of the mitochondrial enzyme, gene structures, chromosomal mapping and comparison with the human orthologs
Q37600502Serial segmental duplications during primate evolution result in complex human genome architecture
Q35784798Structure and evolution of the Smith-Magenis syndrome repeat gene clusters, SMS-REPs.

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