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November 2007 - Volume 44 - 11
Review
Original articles
Short report
Letters to JMG
Review
Molecular pathogenesis of Wilson and Menkes disease: correlation of mutations with molecular defects and disease phenotypes
(23 August, 2007)
Free
P
de Bie
,
P
Muller
,
C
Wijmenga
,
L W J
Klomp
Original articles
Estimating risks of common complex diseases across genetic and environmental factors: the example of Crohn disease
(27 July, 2007)
C M
Lewis
,
S C L
Whitwell
,
A
Forbes
,
J
Sanderson
,
C G
Mathew
,
T M
Marteau
Factors associated with
HD
CAG repeat instability in Huntington disease
(27 July, 2007)
V C
Wheeler
,
F
Persichetti
,
S M
McNeil
,
J S
Mysore
,
S S
Mysore
,
M E
MacDonald
,
R H
Myers
,
J F
Gusella
,
N S
Wexler
,
The US–Venezuela Collaborative Research Group
High proportion of large genomic deletions and a genotype–phenotype update in 80 unrelated families with juvenile polyposis syndrome
(14 September, 2007)
S
Aretz
,
D
Stienen
,
S
Uhlhaas
,
M
Stolte
,
M M
Entius
,
S
Loff
,
W
Back
,
A
Kaufmann
,
K-M
Keller
,
S H
Blaas
,
R
Siebert
,
S
Vogt
,
S
Spranger
,
E
Holinski-Feder
,
L
Sunde
,
P
Propping
,
W
Friedl
A genome-wide scan for genes involved in primary vesicoureteric reflux
(27 July, 2007)
H
Kelly
,
C M
Molony
,
J M
Darlow
,
M E
Pirker
,
A
Yoneda
,
A J
Green
,
P
Puri
,
D E
Barton
Short report
Blood-derived gene-expression profiling in unravelling susceptibility to recessive disease
(27 July, 2007)
P
Vahteristo
,
A
Kokko
,
O
Saksela
,
K
Aittomäki
,
L A
Aaltonen
Letters to JMG
A novel hearing loss-related mutation occurring in the
GJB2
basal promoter
(27 July, 2007)
T D
Matos
,
H
Caria
,
H
Simões-Teixeira
,
T
Aasen
,
R
Nickel
,
D J
Jagger
,
A
O’Neill
,
D P
Kelsell
,
G
Fialho
Germline E-cadherin mutations in familial lobular breast cancer
(27 July, 2007)
S
Masciari
,
N
Larsson
,
J
Senz
,
N
Boyd
,
P
Kaurah
,
M J
Kandel
,
L N
Harris
,
H C
Pinheiro
,
A
Troussard
,
P
Miron
,
N
Tung
,
C
Oliveira
,
L
Collins
,
S
Schnitt
,
J E
Garber
,
D
Huntsman
Direct contact in inviting high-risk members of hereditary colon cancer families to genetic counselling and DNA testing
(14 July, 2007)
K
Aktan-Collan
,
A
Haukkala
,
K
Pylvänäinen
,
H J
Järvinen
,
L A
Aaltonen
,
P
Peltomäki
,
E
Rantanen
,
H
Kääriäinen
,
J-P
Mecklin
Mutations in the
AP1S2
gene encoding the sigma 2 subunit of the adaptor protein 1 complex are associated with syndromic X-linked mental retardation with hydrocephalus and calcifications in basal ganglia
(6 July, 2007)
Y
Saillour
,
G
Zanni
,
V
Des Portes
,
D
Heron
,
L
Guibaud
,
M T
Iba-Zizen
,
J L
Pedespan
,
K
Poirier
,
L
Castelnau
,
C
Julien
,
C
Franconnet
,
D
Bonthron
,
M E
Porteous
,
J
Chelly
,
T
Bienvenu
Issue Information
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Front Matter (PDF)