R1 DNA Structure and Properties
Chapter 10, pp. 274-293 , William Klug and Michael Cummings,
"Concepts of Genetics." 45h ed., Prentice-Hall, Inc.,
1997
R2 Mapping by Meiotic Recombination
Chapter 5, pp. 123-144 , Griffiths and others,"Introduction
to Genetic Analysis." 6th ed., W. H. Freeman Co., 1996.
R3 Cloning Bacterial Genes by Complementation
Adapted from Stanley Bower and others, "Cloning,
sequencing, and characterization of the Bacillus subtilis
biotin biosynthetic operon." J. Bacteriology vol. 178
(1996) pages 4122- 4130.
R4 Bacterial Virus Genetics
Walton L. Fangman, "Complementation and intragenic
recombination with a bacterial virus."
R5 Mutations in a Human Gene Resulting in Stops, Frameshifts
and a Splicing Defect
Adapted from Anna Maria Barbieri and others, "Seven
novel additional small mutations and a new alternative splicing
in the human dystrophin gene ......" Eur. J. Human Genet.
vol. 4 (1996) pages 183-187.
R6 Meiotic Linkage Analysis with Human Pedigrees
Natalie Angier, "Scientists zero in on gene tied
to prostate cancer." The New York Times, November 22, 1996.
Walton L. Fangman and Katherine Kolor, "Quantitative
analysis of linkage with human pedigrees."
R7 Cloning and Sequence Analysis of a Human Disease Gene
Adapted from Toshio Mochizuki and others, "PDK2,
a gene for polycystic kidney disease that encodes an integral
membrane protein." Science vol. 272 (1996) pages 1339-1342.
R8 Mitochondrial DNA Inheritance
An article relevant to this topic will be handed-out
if an appropriate one is found.
R9 Analysis of a Bacterial Promoter
Adapted from Teresa J. Kenny and Gordon Churchward, "Genetic
analysis of theMycobacterium smegmatis rpsL promoter."
J. Bacteriology vol. 178 (1996) pages 3564- 3571.
R10 Regulation of a Bacterial Gene
Adapted from Frieder Schock and Michael Dahl, "Expression
of the tre operon of Bacillus subtilis 168 is
regulated by the repressor TreR." J. Bacteriology vol.
178 (1996) pages 4576-4581.
R11 Mutations Causing Defects in Human Development
Adapted from Yatsuteru Muragaki and others, "Altered
growth and branching patterns in synpolydactyly caused by mutations
in HOXD13." Science vol. 272 (1996) pages 548-551.