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BMJ Journals
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Journal of Medical Genetics
CLINICAL
Immunology (including allergy)
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Immunology (including allergy)
Genetic influences on the circulating cytokines involved in osteoclastogenesis
G
Livshits
,
I
Pantsulaia
,
S
Trofimov
,
E
Kobyliansky
Journal of Medical Genetics
Jun 2004,
41
(6)
e76;
DOI:
10.1136/jmg.2003.014373
Laugier-Hunziker syndrome: an important differential diagnosis for Peutz-Jeghers syndrome
A K
Lampe
,
P J
Hampton
,
K
Woodford-Richens
,
I
Tomlinson
,
C M
Lawrence
,
F S
Douglas
Journal of Medical Genetics
Jun 2003,
40
(6)
e77;
DOI:
10.1136/jmg.40.6.e77
A unique form of hypodontia seen in Vietnamese patients: cinical and molecular analysis
S A
Frazier-Bowers
,
K Y
Pham
,
E V
Le
,
A C
Cavender
,
H
Kapadia
,
T M
King
,
D M
Milewicz
,
R N
D'Souza
Journal of Medical Genetics
Jun 2003,
40
(6)
e79;
DOI:
10.1136/jmg.40.6.e79
Hereditary duplication of proximal chromosome 1q (q11q22) in a patient with T lymphoblastic lymphoma/leukaemia: a family study using G banding and comparative genomic hybridisation
N P H
Chan
,
M H L
Ng
,
S H
Cheng
,
V
Lee
,
K S
Tsang
,
T T
Lau
,
C K
Li
Journal of Medical Genetics
Dec 2002,
39
(12)
e79;
DOI:
10.1136/jmg.39.12.e79
Evidence of differing genotypic effects of PPARα in women and men
Q H
Khan
,
D E
Pontefract
,
S
Iyengar
,
S
Ye
Journal of Medical Genetics
Jun 2004,
41
(6)
e79;
DOI:
10.1136/jmg.2003.014407
Alström syndrome: confirmation of linkage to chromosome 2p12-13 and phenotypic heterogeneity in three affected sibs
URS
ZUMSTEG
,
PATRICK Y
MULLER
,
ANDRÉ R
MISEREZ
Journal of Medical Genetics
Jul 2000,
37
(7)
e8;
DOI:
10.1136/jmg.37.7.e8
Lack of founder haplotype for the rapsyn N88K mutation: N88K is an ancient founder mutation or arises from multiple founders
K
Ohno
,
A G
Engel
Journal of Medical Genetics
Jan 2004,
41
(1)
e8;
DOI:
10.1136/jmg.2003.012245
Genetic information but not termination: pregnant women's attitudes and willingness to pay for carrier screening for deafness genes
M
Ryan
,
Z
Miedzybrodzka
,
L
Fraser
,
M
Hall
Journal of Medical Genetics
Jun 2003,
40
(6)
e80;
DOI:
10.1136/jmg.40.6.e80
Frequency of mutations in the early growth response 2 gene associated with peripheral demyelinating neuropathies
N
Vandenberghe
,
M
Upadhyaya
,
A
Gatignol
,
L
Boutrand
,
M
Boucherat
,
G
Chazot
,
A
Vandenberghe
,
P
Latour
Journal of Medical Genetics
Dec 2002,
39
(12)
e81;
DOI:
10.1136/jmg.39.12.e81
Case report: a subject with a mutation in the ATG start codon of L-ferritin has no haematological or neurological symptoms
L
Cremonesi
,
A
Cozzi
,
D
Girelli
,
F
Ferrari
,
I
Fermo
,
B
Foglieni
,
S
Levi
,
C
Bozzini
,
M
Camparini
,
M
Ferrari
,
P
Arosio
Journal of Medical Genetics
Jun 2004,
41
(6)
e81;
DOI:
10.1136/jmg.2003.011718
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