Now showing items 1-4 of 4

An African-American cystic fibrosis patient homozygous for a novel frameshift mutation associated with reduced CFTR mRNA levels

Smit, Lisa S.; Nasr, Samya Z.; Iannuzzi, Michael C.; Collins, Francis S. (Wiley Subscription Services, Inc., A Wiley Company, 1993)

(327.9KB)
Characterization of an intron 12 splice donor mutation in the cystic fibrosis transmembrane conductance regulator (CFTR) gene

Strong, Theresa V.; Smit, Lisa S.; Nasr, Samya Z.; Wood, Deborah L.; Cole, Jeffrey L.; Iannuzzi, Michael C.; Stern, Robert C.; Collins, Francis S. (Wiley Subscription Services, Inc., A Wiley Company, 1992)

(661.8KB)
Physical mapping of the cystic fibrosis region by pulsed-field gel electrophoresis

Drumm, Mitchell L.; Smith, Cassandra L.; Dean, Michael; Cole, Jeffery L.; Iannuzzi, Michael C.; Collins, Francis S. (Elsevier, 1988-05)

(1.9MB)
Prenatal diagnosis and linkage disequilibrium with cystic fibrosis for markers surrounding D7S8

Romeo, Giovanni; Dean, Michael; Lynch, Jennifer; Amos, Jean A.; Ferrari, Maurizio; Halley, Dicky; Russo, Silvia; Finn, Paula B.; Iannuzzi, Michael C.; Collins, Francis S.; Devoto, Marcella; Oostra, Ben; Weir, Bruce S.; Ward, Ken (Springer-Verlag, 1990-08)

(384.2KB)

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