Identification and characterization of mouse orthologs of the AMMECR1 and FACL4 genes deleted in AMME syndrome: Orthology of Xq22.3 and MmuXF1-F3

Cytogenetics and Cell Genetics

Volumn 88, Issue 3-4, 2000, Pages 259-263

  Vitelli, F ^c   Meloni, I ^c   Fineschi, S ^c   Favara, F ^c   Tiziana Storlazzi, C ^a   Rocchi, M ^a   Renieri, Alessandra ^b  

^a Istituto di Genetica   (Italy)

^b UNIVERSITY HOSPITAL OF SIENA   (Italy)

^c NONE

Author keywords

[No Author keywords available]

Indexed keywords

CONTIG;

ALPORT SYNDROME; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CELLULAR DISTRIBUTION; CHROMOSOME ARM; FEMALE; HEREDITARY ELLIPTOCYTOSIS; HUMAN; MALE; MENTAL DEFICIENCY; MIDFACE HYPOPLASIA; MOLECULAR CLONING; MOUSE; NONHUMAN; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; SEQUENCE HOMOLOGY; X CHROMOSOME;

MURINAE;

EID: 0034023784     PISSN: 03010171     EISSN: None     Source Type: Journal    
DOI: 10.1159/000015533     Document Type: Article

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