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3 Article(s) on File
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Haplotype analysis improves molecular diagnostics of autosomal recessive polycystic kidney disease
Consugar MB,
Anderson SA,
Rossetti S,
Pankratz S,
Ward CJ,
Torra R,
Coto E,
El-Youssef M,
Kantarci S,
Utsch B,
Hildebrandt F,
Sweeney WE,
Avner ED,
Torres VE,
Cunningham JM,
Harris PC

American Journal of Kidney Diseases
  45 (1): 77-87; Jan 2005  
[Abstract]
[DOI] [Full Text] [PDF]

Haplotype analysis in autosomal recessive polycystic kidney disease (ARPKD) families and the determination of allele frequencies of used markers in the Turkish population
Kantarci S,
Apak MY,
Eraslan S,
Nayir A,
Kayserili H,
Kirdar B

American Journal of Human Genetics
  73 (5): 477-477; Nov 2003  
[Full Text]

Joubert syndrome: a patient with a de novo t(2;22)(q13;q11.1)
Hatchwell E,
Tommerup N,
Kristoffersson U,
Stanyon R,
Kantarci S

American Journal of Human Genetics
  73 (5): 566-566; Nov 2003  
[Full Text]


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