|
|
| 1. |
National haemophilia B molecular genetic register. |
| |
Journal of Medical Genetics,
Volume 29,
Issue 9,
1992,
Page 601-601
RHarris,
Preview
|
PDF (136KB)
|
|
ISSN:0022-2593
出版商:J Med Genet
年代:1992
数据来源: BMJ
|
| 2. |
A new strategy for the genetic counselling of diseases of marked mutational heterogeneity: haemophilia B as a model. |
| |
Journal of Medical Genetics,
Volume 29,
Issue 9,
1992,
Page 602-607
FGiannelli,
SSaad,
A JMontandon,
D RBentley,
P MGreen,
Preview
|
PDF (1176KB)
|
|
ISSN:0022-2593
出版商:J Med Genet
年代:1992
数据来源: BMJ
|
| 3. |
X inactivation as a mechanism of selection against lethal alleles: further investigation of incontinentia pigmenti and X linked lymphoproliferative disease. |
| |
Journal of Medical Genetics,
Volume 29,
Issue 9,
1992,
Page 608-614
AHarris,
JCollins,
DVetrie,
CCole,
MBobrow,
Preview
|
PDF (1393KB)
|
|
ISSN:0022-2593
出版商:J Med Genet
年代:1992
数据来源: BMJ
|
| 4. |
Phenotype-genotype correlations in X linked retinitis pigmentosa. |
| |
Journal of Medical Genetics,
Volume 29,
Issue 9,
1992,
Page 615-623
JKaplan,
APelet,
CMartin,
ODelrieu,
SAymé,
DBonneau,
M LBriard,
AHanauer,
LLarget-Piet,
PLefrançois,
Preview
|
PDF (1185KB)
|
|
ISSN:0022-2593
出版商:J Med Genet
年代:1992
数据来源: BMJ
|
| 5. |
Chromosomal localisation of a pseudoautosomal growth gene(s). |
| |
Journal of Medical Genetics,
Volume 29,
Issue 9,
1992,
Page 624-628
TOgata,
CPetit,
GRappold,
NMatsuo,
TMatsumoto,
PGoodfellow,
Preview
|
PDF (1180KB)
|
|
ISSN:0022-2593
出版商:J Med Genet
年代:1992
数据来源: BMJ
|
| 6. |
Non-specific X linked mental retardation with aphasia exhibiting genetic linkage to chromosomal region Xp11. |
| |
Journal of Medical Genetics,
Volume 29,
Issue 9,
1992,
Page 629-634
G NWilson,
C SRichards,
KKatz,
G SBrookshire,
Preview
|
PDF (1290KB)
|
|
ISSN:0022-2593
出版商:J Med Genet
年代:1992
数据来源: BMJ
|
| 7. |
The acrocallosal syndrome and Greig syndrome are not allelic disorders. |
| |
Journal of Medical Genetics,
Volume 29,
Issue 9,
1992,
Page 635-637
L ABrueton,
K AChotai,
Lvan Herwerden,
ASchinzel,
R MWinter,
Preview
|
PDF (431KB)
|
|
ISSN:0022-2593
出版商:J Med Genet
年代:1992
数据来源: BMJ
|
| 8. |
Multipoint mapping of adult onset polycystic kidney disease (PKD1) on chromosome 16. |
| |
Journal of Medical Genetics,
Volume 29,
Issue 9,
1992,
Page 638-641
P MPignatelli,
S EPound,
A DCarothers,
A MMacnicol,
P LAllan,
M LWatson,
A FWright,
Preview
|
PDF (732KB)
|
|
ISSN:0022-2593
出版商:J Med Genet
年代:1992
数据来源: BMJ
|
| 9. |
Mutation analysis of 184 cystic fibrosis families in Wales. |
| |
Journal of Medical Genetics,
Volume 29,
Issue 9,
1992,
Page 642-646
JCheadle,
JMyring,
Lal-Jader,
LMeredith,
Preview
|
PDF (966KB)
|
|
ISSN:0022-2593
出版商:J Med Genet
年代:1992
数据来源: BMJ
|
| 10. |
Identification of a new DMD gene deletion by ectopic transcript analysis. |
| |
Journal of Medical Genetics,
Volume 29,
Issue 9,
1992,
Page 647-651
FRininsland,
AHahn,
SNiemann-Seyde,
RSlomski,
FHanefeld,
JReiss,
Preview
|
PDF (1177KB)
|
|
ISSN:0022-2593
出版商:J Med Genet
年代:1992
数据来源: BMJ
|
|
首页
