Information regarding Cystic Fibrosis, the types of research being performed to finds its cure.  Learn more about gene therapy, and treatments for Cystic Fibrosis as well as volunteering opportunities.
The Center has many research laboratories dedicated to finding a cure for Cystic Fibrosis.  Meet the different lab directors, their lab members and the laboratories particular focus.
A complete list of publications from the Centers lab directors that are related to Cystic Fibrosis.
Apply for open positions at the Cystic Fibrosis Research Development Center.
Visit other websites of organizations and associations affiliated with Cystic Fibrosis.
Letter from the Director addressing the Centers continued plan for the future.




















Garry Richard Cutting, M.D.

Garry Home|Publications|Book Chapters | Lab Members



Garry Richard Cutting, M.D.
Professor of Pediatric and Medicine
Aetna/U.S. Healthcare Professor of Medical Genetics
Director, Residency and Postdoctoral Training Program in Medical Genetics
Director, DNA Diagnostic Laboratory
The Johns Hopkins University School of Medicine
Baltimore, MD 21205


Garry Cutting


Cutting GR, Antonarakis SE, Youssoufian H and Kazazian H Jr.  The accuracy and limitations of Pulsed Field Gel Electrophoresis in sizing partial deletions of the factor VIII gene.  Molecular Biology and Medicine (1988), 5:173-184.

  Cutting GR, Kazazian H Jr, Antonarakis SE, Killen PD, Yamada Y and Francomano CA.  Macrorestriction mapping of human collagen genes COL4A1 and COL4A2 on chromosome 13q34.  Genomics (1988), 3:256-263.
  Jabs EW, Goble CA, Cutting GR.  The macromolecular organization of human centromeric region reveals high frequency, polymorphic macro-DNA repeats.  Proc Natl Acad Sci (USA) (1989), 86:202-206.
  Cutting GR, Antonarakis SE, Beutow KH, Kasch LM, Rosenstein BJ, Kazazian H Jr.  Analysis of DNA polymorphism haplotypes linked to the Cystic Fibrosis locus in North American Black and Caucasian families support the existence of multiple mutations of the Cystic Fibrosis gene.  Am J Hum Genet (1989), 44:307-318.
  Cutting GR, McGinniss MJ, Kasch LM, Tsipouras P, Antonarakis SE.  Physical mapping by PFGE localizes the COL3A1 and COL5A2 genes to a 35kb region on chromosome 2.  Genomics (1990), 8:407-410.

 Cutting GR, Kasch LM.  Worldwide survey of the  deltaF508 mutation-report from the Cystic Fibrosis Genetic Analysis Consortium.  Am J Hum Genet (1990), 47:354-359.

  Cutting GR, Kasch LM, Rosenstein BJ, Tsui L-C, Kazazian H and Antonarakis SE.  Two patients with Cystic Fibrosis, nonsense mutations in each Cystic Fibrosis gene, and mild pulmonary disease.  New Engl J Med (1990), 323:1685-1689.
  Cutting GR, Kasch LM, Rosenstein BJ, Zielensky J, Tsui L-C, Antonarakis SE, Kazazian H Jr.  A cluster of Cystic Fibrosis mutations in the first nucleotide binding fold domain of the Cystic Fibrosis conductance regulator protein.  Nature (1990), 346:366-369.
  Beaudet AL, Perciaccante RG, Cutting GR. Homozygous nonsense mutation causing cystic fibrosis with uniparental disomy. Am. J. Hum. Genet. (1991) 48:1213.
  Nunes V, Gaona MC, Mana P, Casals T, Cutting GR, Estivill X:  Prenatal diagnosis of cystic fibrosis by simultaneous analysis of two different mutations.  Prenatal Diagnosis (1991) 11:671-672. 
  McColley SA, Rosenstein BJ, Cutting GR.  Differences in Expression of Cystic Fibrosis in Blacks and Whites.  Am J Dis Child (1991), 145:94-97.

Publications Next

615 N. Wolfe Street, Baltimore, MD 21205