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| 1. |
Splotch locus mouse mutants: models for neural tube defects and Waardenburg syndrome type I in humans. |
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Journal of Medical Genetics,
Volume 29,
Issue 3,
1992,
Page 145-151
C EMoase,
D GTrasler,
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ISSN:0022-2593
出版商:J Med Genet
年代:1992
数据来源: BMJ
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| 2. |
Family history of breast cancer: how important is it? |
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Journal of Medical Genetics,
Volume 29,
Issue 3,
1992,
Page 152-153
D TBishop,
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PDF (242KB)
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ISSN:0022-2593
出版商:J Med Genet
年代:1992
数据来源: BMJ
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| 3. |
Family history and risk of breast cancer. |
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Journal of Medical Genetics,
Volume 29,
Issue 3,
1992,
Page 154-157
R SHoulston,
EMcCarter,
SParbhoo,
J HScurr,
JSlack,
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PDF (689KB)
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ISSN:0022-2593
出版商:J Med Genet
年代:1992
数据来源: BMJ
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| 4. |
Epidemiology of breast cancer in families in Iceland. |
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Journal of Medical Genetics,
Volume 29,
Issue 3,
1992,
Page 158-164
HTulinius,
HSigvaldason,
GOlafsdóttir,
LTryggvadóttir,
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PDF (1267KB)
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ISSN:0022-2593
出版商:J Med Genet
年代:1992
数据来源: BMJ
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| 5. |
Prenatal prediction of spinal muscular atrophy. |
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Journal of Medical Genetics,
Volume 29,
Issue 3,
1992,
Page 165-170
R JDaniels,
G KSuthers,
K EMorrison,
N HThomas,
M JFrancis,
C GMathew,
SLoughlin,
AHeiberg,
DWood,
VDubowitz,
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PDF (1119KB)
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ISSN:0022-2593
出版商:J Med Genet
年代:1992
数据来源: BMJ
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| 6. |
Prenatal prediction of Werdnig-Hoffmann disease using linked polymorphic DNA probes. |
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Journal of Medical Genetics,
Volume 29,
Issue 3,
1992,
Page 171-174
JMelki,
SAbdelhak,
PBurlet,
VRaclin,
JKaplan,
RSpiegel,
SGilgenkrantz,
NPhilip,
M LChauvet,
YDumez,
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PDF (597KB)
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ISSN:0022-2593
出版商:J Med Genet
年代:1992
数据来源: BMJ
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| 7. |
An intrachromosomal insertion causing 5q22 deletion and familial adenomatous polyposis coli in two generations. |
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Journal of Medical Genetics,
Volume 29,
Issue 3,
1992,
Page 175-179
ICross,
JDelhanty,
PChapman,
L VBowles,
DGriffin,
JWolstenholme,
MBradburn,
JBrown,
CWood,
AGunn,
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PDF (1046KB)
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ISSN:0022-2593
出版商:J Med Genet
年代:1992
数据来源: BMJ
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| 8. |
Prenatal diagnosis and presymptomatic detection of neurofibromatosis type 1. |
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Journal of Medical Genetics,
Volume 29,
Issue 3,
1992,
Page 180-183
MUpadhyaya,
AFryer,
JMacMillan,
WBroadhead,
S MHuson,
P SHarper,
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PDF (666KB)
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ISSN:0022-2593
出版商:J Med Genet
年代:1992
数据来源: BMJ
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| 9. |
Clinical variability of type 1 neurofibromatosis: is there a neurofibromatosis-Noonan syndrome? |
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Journal of Medical Genetics,
Volume 29,
Issue 3,
1992,
Page 184-187
H JStern,
H MSaal,
J SLee,
P RFain,
D EGoldgar,
K NRosenbaum,
D FBarker,
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PDF (915KB)
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ISSN:0022-2593
出版商:J Med Genet
年代:1992
数据来源: BMJ
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| 10. |
Absence of linkage of Noonan syndrome to the neurofibromatosis type 1 locus. |
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Journal of Medical Genetics,
Volume 29,
Issue 3,
1992,
Page 188-190
MSharland,
RTaylor,
M APatton,
SJeffery,
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PDF (399KB)
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ISSN:0022-2593
出版商:J Med Genet
年代:1992
数据来源: BMJ
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