Detection of a megabase deletion in a patient with branchio-oto-renal syndrome (BOR) and tricho-rhino-phalangeal syndrome (TRPS): Implications for mapping and cloning the BOR gene

Genomics

Volumn 31, Issue 2, 1996, Pages 201-206

  Gu, Jessie Z ^a   Wagner, Michael J ^b   Haan, Eric A ^c   Wells, Dan E ^a  

^a University of Houston   (United States)

^b GLAXOSMITHKLINE   (United States)

^c WOMEN S AND CHILDREN S HOSPITAL   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

ANIMAL CELL; ARTICLE; CHROMOSOME 8Q; CLINICAL FEATURE; CRUSH SYNDROME; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DELETION; GENE FUNCTION; GENE LOCATION; GENE MAPPING; HUMAN; KIDNEY MALFORMATION; MOLECULAR CLONING; PRIORITY JOURNAL;

ANIMALIA;

EID: 0030062521     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.1996.0032     Document Type: Article

References (23)

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