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| 1. |
A possible human homologue for the mouse mutant disorganisation. |
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Journal of Medical Genetics,
Volume 26,
Issue 7,
1989,
Page 417-420
R MWinter,
DDonnai,
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PDF (727KB)
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ISSN:0022-2593
出版商:J Med Genet
年代:1989
数据来源: BMJ
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| 2. |
Disorganisation: a model for 'early amnion rupture'? |
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Journal of Medical Genetics,
Volume 26,
Issue 7,
1989,
Page 421-425
DDonnai,
R MWinter,
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PDF (1250KB)
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ISSN:0022-2593
出版商:J Med Genet
年代:1989
数据来源: BMJ
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| 3. |
Testing for cystic fibrosis using allelic association. |
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Journal of Medical Genetics,
Volume 26,
Issue 7,
1989,
Page 426-430
A JIvinson,
A PRead,
RHarris,
MSuper,
MSchwarz,
JClayton Smith,
RElles,
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PDF (779KB)
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ISSN:0022-2593
出版商:J Med Genet
年代:1989
数据来源: BMJ
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| 4. |
T cell receptor beta chain polymorphisms are associated with cystic fibrosis. |
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Journal of Medical Genetics,
Volume 26,
Issue 7,
1989,
Page 431-433
S AMcMillan,
A JHill,
C AGraham,
N CNevin,
A CFay,
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PDF (508KB)
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ISSN:0022-2593
出版商:J Med Genet
年代:1989
数据来源: BMJ
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| 5. |
Blepharophimosis plus ovarian failure: a likely candidate for a contiguous gene syndrome. |
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Journal of Medical Genetics,
Volume 26,
Issue 7,
1989,
Page 434-438
ASmith,
I SFraser,
R PShearman,
PRussell,
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PDF (676KB)
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ISSN:0022-2593
出版商:J Med Genet
年代:1989
数据来源: BMJ
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| 6. |
Fragile X testing in a diagnostic cytogenetics laboratory. |
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Journal of Medical Genetics,
Volume 26,
Issue 7,
1989,
Page 439-442
L EVoullaire,
G CWebb,
MLeversha,
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PDF (560KB)
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ISSN:0022-2593
出版商:J Med Genet
年代:1989
数据来源: BMJ
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| 7. |
Intelligence and cognitive profile in the fra(X) syndrome: a longitudinal study in 18 fra(X) boys. |
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Journal of Medical Genetics,
Volume 26,
Issue 7,
1989,
Page 443-446
L MCurfs,
GSchreppers-Tijdink,
AWiegers,
MBorghgraef,
J PFryns,
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PDF (555KB)
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ISSN:0022-2593
出版商:J Med Genet
年代:1989
数据来源: BMJ
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| 8. |
Severe Silver-Russell syndrome. |
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Journal of Medical Genetics,
Volume 26,
Issue 7,
1989,
Page 447-451
DDonnai,
EThompson,
JAllanson,
MBaraitser,
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PDF (1191KB)
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ISSN:0022-2593
出版商:J Med Genet
年代:1989
数据来源: BMJ
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| 9. |
Differential expression of the ICF (immunodeficiency, centromeric heterochromatin, facial anomalies) mutation in lymphocytes and fibroblasts. |
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Journal of Medical Genetics,
Volume 26,
Issue 7,
1989,
Page 452-456
PMaraschio,
RTupler,
EDainotti,
MPiantanida,
GCazzola,
LTiepolo,
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PDF (804KB)
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ISSN:0022-2593
出版商:J Med Genet
年代:1989
数据来源: BMJ
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| 10. |
Kyphomelic dysplasia. |
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Journal of Medical Genetics,
Volume 26,
Issue 7,
1989,
Page 457-461
I KTemple,
E MThompson,
C MHall,
GBridgeman,
M EPembrey,
Preview
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PDF (1304KB)
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ISSN:0022-2593
出版商:J Med Genet
年代:1989
数据来源: BMJ
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