FXY2/MID2, a gene related to the X-linked Opitz syndrome gene FXY/MID1, maps to Xq22 and encodes a FNIII domain-containing protein that associates with microtubules

Genomics

Volumn 62, Issue 3, 1999, Pages 385-394

  Perry, Jo ^a   Short, Kieran M ^b   Romer, Justyna T ^a   Swift, Sally ^a   Cox, Timothy C ^b   Ashworth, Alan ^a  

^a INSTITUTE OF CANCER RESEARCH   (United Kingdom)

^b UNIVERSITY OF ADELAIDE   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA TUBULIN; COMPLEMENTARY DNA; MICROTUBULE ASSOCIATED PROTEIN; PLASMID DNA;

ANIMAL CELL; ARTICLE; CELL FRACTIONATION; CHROMOSOMAL LOCALIZATION; CHROMOSOME XQ; CLEFT LIP PALATE; CONGENITAL HEART MALFORMATION; GENE MAPPING; HUMAN; HUMAN CELL; MICROTUBULE; MULTIPLE MALFORMATION SYNDROME; NONHUMAN; NUCLEOTIDE SEQUENCE; OPITZ SYNDROME; PRIORITY JOURNAL; SYNDROME DELINEATION; X CHROMOSOME LINKED DISORDER;

ANIMALIA;

EID: 0033572528     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.1999.6043     Document Type: Article

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