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| 1. |
Molecular and cytogenetic studies of the Prader-Willi syndrome. |
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Journal of Medical Genetics,
Volume 28,
Issue 10,
1991,
Page 649-654
R JTrent,
FVolpato,
ASmith,
RLindeman,
M KWong,
GWarne,
EHaan,
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ISSN:0022-2593
出版商:J Med Genet
年代:1991
数据来源: BMJ
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| 2. |
Genetic counselling in facioscapulohumeral muscular dystrophy. |
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Journal of Medical Genetics,
Volume 28,
Issue 10,
1991,
Page 655-664
P WLunt,
P SHarper,
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PDF (1260KB)
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ISSN:0022-2593
出版商:J Med Genet
年代:1991
数据来源: BMJ
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| 3. |
A closely linked DNA marker for facioscapulohumeral disease on chromosome 4q. |
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Journal of Medical Genetics,
Volume 28,
Issue 10,
1991,
Page 665-671
MUpadhyaya,
P WLunt,
MSarfarazi,
WBroadhead,
JDaniels,
MOwen,
P SHarper,
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PDF (825KB)
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ISSN:0022-2593
出版商:J Med Genet
年代:1991
数据来源: BMJ
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| 4. |
Sex ratio of the mutation frequencies in haemophilia A: coagulation assays and RFLP analysis. |
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Journal of Medical Genetics,
Volume 28,
Issue 10,
1991,
Page 672-680
A HBröcker-Vriends,
F RRosendaal,
J Cvan Houwelingen,
EBakker,
G Jvan Ommen,
J Jvan de Kamp,
EBriët,
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PDF (1370KB)
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ISSN:0022-2593
出版商:J Med Genet
年代:1991
数据来源: BMJ
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| 5. |
Linkage analysis in adenomatous polyposis coli: the use of four closely linked DNA probes in 20 UK families. |
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Journal of Medical Genetics,
Volume 28,
Issue 10,
1991,
Page 681-685
M BCachon-Gonzalez,
J DDelhanty,
JBurn,
KTsioupra,
M BDavis,
JAttwood,
PChapman,
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PDF (638KB)
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ISSN:0022-2593
出版商:J Med Genet
年代:1991
数据来源: BMJ
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| 6. |
Silent mutations in the phenylalanine hydroxylase gene as an aid to the diagnosis of phenylketonuria. |
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Journal of Medical Genetics,
Volume 28,
Issue 10,
1991,
Page 686-690
LKalaydjieva,
BDworniczak,
CAulehla-Scholz,
MDevoto,
GRomeo,
MSturhmann,
VKucinskas,
VYurgelyavicius,
JHorst,
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PDF (771KB)
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ISSN:0022-2593
出版商:J Med Genet
年代:1991
数据来源: BMJ
|
| 7. |
A male with type I orofaciodigital syndrome. |
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Journal of Medical Genetics,
Volume 28,
Issue 10,
1991,
Page 691-694
JGoodship,
JPlatt,
RSmith,
JBurn,
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PDF (929KB)
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ISSN:0022-2593
出版商:J Med Genet
年代:1991
数据来源: BMJ
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| 8. |
Miller syndrome (postaxial acrofacial dysostosis): further evidence for autosomal recessive inheritance and expansion of the phenotype. |
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Journal of Medical Genetics,
Volume 28,
Issue 10,
1991,
Page 695-700
A LOgilvy-Stuart,
A CParsons,
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PDF (1681KB)
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ISSN:0022-2593
出版商:J Med Genet
年代:1991
数据来源: BMJ
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| 9. |
A new form of autosomal dominant arthrogryposis. |
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Journal of Medical Genetics,
Volume 28,
Issue 10,
1991,
Page 701-703
M MLai,
M ATettenborn,
J GHall,
L JSmith,
A CBerry,
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PDF (717KB)
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ISSN:0022-2593
出版商:J Med Genet
年代:1991
数据来源: BMJ
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| 10. |
Cerebrocostomandibular syndrome in four sibs, two pairs of twins. |
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Journal of Medical Genetics,
Volume 28,
Issue 10,
1991,
Page 704-707
VDrossou-Agakidou,
AAndreou,
VSoubassi-Griva,
MPandouraki,
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PDF (1146KB)
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ISSN:0022-2593
出版商:J Med Genet
年代:1991
数据来源: BMJ
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