|
-
ALPER,
J.S. e NATOWICZ, M.R. "On establishing the genetic basis of mental
disease". Trends in Neuroscience,
v.16, 1993, p.387.
-
BROOK,
J.D.; MCCURRACH, M.E.; HARLEY, H.G. et alii. "Molecular basis of myotonic
dystrophy: expansion of a a trinucleotide (CTG) repeat at the 3'end of a
transcript encoding a protein kinase family member". Cell n.68, 1992,
p.799-808.
-
BRUNNER,
H.G.; NELEN, M.; BREAKEFIELD, O.; ROPERS, H. e VAN OOST, B.A. "Abnormal
behavior associated with a point mutation in the structural gene for monoamine
oxidase A". Science, n.258,
1993, p.668.
-
CRABBE,
J.C.; BELKNAP, J.K. e BUCK, K. "Genetic animal models of alcohol and drug
abuse". Science, n.264, 1994,
p.1715-1723.
-
COLLINS,
F.S.; PATRINOS, A.; JORDAN, E.; CHAKRAVARTI, A. GESTELAND R.; WALTERS, LEROY et
alii. New goals for the U.S. human genome project. 1998, p. 1.998-2.003.
-
DAWKINS,
R. "Arresting evidence". Sciences,
1998, p.20-25.
-
HAMER,
D.H. "The heritability of happiness". Nature Genetics, n.14, 1996, p.125-126.
-
HARLEY,
G.H.; BROOK, J.D.; RUNDLE, S.A; CROW, S.; REARDON, W.; BUCKLER, A.J.; HARPER,
P.S. et alii ."Expansion of an unstable DNA region and phenotypic
variation in myotonic dystrophy". Nature,
n.355, 1992, p.545-546.
-
HEIL,
A.; TEUFEL, A.; PETRI, S.; STOBER, G.; RIEDERER, P.; BENGEl, D. e LESCH, K.P.
"Allelic variation of human serotonin transporter gene expression". Journal of Neurochemics, n.66, 1996,
p.2621-2626.
-
HU,
S.; PATTATUCCI, A.M.; PATTERSON, C.; LIN, L.; FULKER, D.W.; CHERNY, S.C.;
KRUGLYACK, L. e HAMER, D.S. "Linkage between sexual orientation and
chromosome Xq28 in males but not in females". Nature Genetics, n.11, 1995, p.248-256.
-
KREMER,
B.; GOLDBERG, P.; ANDREW, S.E.; THEILMANN, J.; TELENIUS, H.; ZEISLER, J.;
SQUITIERI, F. et alii. "A worldwide study of the Huntington's disease
mutation: the sensitivity and specifity of measuring CAG repeats". N. Engl. J. Med., n.330, 1994,
p.1401-1406.
-
LaBUDA,
M.C.; GOTTESMAN II e PAULS, D.L. "The usefulness of twin studies for
exploring the etiology of childhood and adolescent psychiatric disorders".
Am. J. Med. Genet., n.48, 1993, p.47-59.
-
LESCH,
K.P.; BENGEL, D.; HEILS, A.; SABOL, S.Z.; GREENBERG, B.D.; PETRI, S.; BENJAMIN,
J.; MULLER, C.R.; HAMER, D.H. e MURPHY, D.L. "Association of
anxiety-related traits with a polymorphism in the serotonin transporter gene
regulatory region". Science, n.
274, 1996, p.1527-1531.
-
MALLET,
J.; MELONI, R. e LAURENT, C. "Catecholamine metabolism and psychiatric or
behavioral disorders". Curr.
Opinion. Genet. Develop., n.4, 1994, p.419-426.
-
MANN,
C. "Behavioral genetics in transition". Science, n.264, 1994, p.1.686-1.695.
-
MCKUSICK,
V. e AMBERGER, J.S. "The morbid anatomy of the human genome: chromosomal
location of mutations causing diseases". J. Med. Genet, 1994, p.265-279.
-
NOVAK,
R. "Genetic testing set for takeoff". Science, n.265, 1994, p.464- 467.
-
OLIVEIRA,
J.R.M.; GALLINDO, R.M.; MAIA, L.G.S.; BRITO-MARQUES, P.R.; OTTO, P.A.;
PASSOS-BUENO, M.R.; MORAIS Jr., M.A. e ZATZ, M. "The short variant of the
polymorphism within the promoter region of the serotonin transporter gene is a
risk factor for late onset Alzheimer's disease". Molecular Psychiatry, n.3, 1998, p.438-441.
-
PALMOUR,
R.M.; MULLIGAN, J.; HOWBERT, J.J. e ERVIN, F. "Insigths from model
systems: of monkeys and men: vervets and the genetics of human-like
behaviors". Am. J. Hum. Genet.,
n.61, 1997, p.481-488.
-
PLOMIN,
R.; OWEN, M.J. e MCGUFFIN, P. "The genetic basis of complex human
behavior". Science, n.264, 1994,
p.1.733-1.737.
-
PONDER,
B. "Genetic testing for cancer risk". Science, n.278, 1997, p.1.050-1.054.
-
STATHAM,
H.; GREEN, J.; SNOWDON, C. e FRANCE-DAWSON, M. "Choice of baby's
Sex". Lancet, n.341, 1993, p.564-565
|