Chromosomal mapping of the gene (INPP5A) encoding the 43-kDa membrane-associated inositol polyphosphate 5-phosphatase to 10q26.3 by fluorescence in situ hybridization

Genomics

Volumn 31, Issue 1, 1996, Pages 139-140

  Mitchell, Christina A ^a   Speed, Caroline J ^a   Nicholl, Jillian ^b   Sutherland, Grant R ^b  

^a BOX HILL HOSPITAL   (Australia)

^b WOMEN S AND CHILDREN S HOSPITAL   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

INOSITOL POLYPHOSPHATE; PHOSPHATASE;

ARTICLE; CHROMOSOMAL LOCALIZATION; CHROMOSOME 10Q; CHROMOSOME BAND; CHROMOSOME MAP; FLUORESCENCE IN SITU HYBRIDIZATION; GENE; HUMAN; LOWE SYNDROME; METAPHASE; PRIORITY JOURNAL; X CHROMOSOME;

CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 10; DNA, COMPLEMENTARY; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; LINKAGE (GENETICS); MALE; OCULOCEREBRORENAL SYNDROME; PHOSPHORIC MONOESTER HYDROLASES; X CHROMOSOME;

EID: 0030066953     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.1996.0023     Document Type: Article

References (13)

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