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Results of search for 'au:"Schäfer, A J"', page 2 of 2
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Authors
Agostini, M
Argentaro, A
Barroso, I
Beck, S
Belchetz, P E
Belfroid, A C
Faulstich, H
Foster, J W
Fournier, R E
Franks, P W
Goodfellow, P N
Guioli, S
Kwok, C
Luan, J
O'Rahilly, S
Schafer, A J
Schäfer, A J
Soos, M A
Wareham, N J
Weller, P A
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Actins
Adult
Animals
Base Sequence
Chromosome Mapping
Chromosomes, Human, Pair 17
DNA
DNA-Binding Proteins
Disorders of Sex Development
Female
Genetic Linkage
High Mobility Group Proteins
Humans
Hybrid Cells
Male
Mutation
Phenotype
Transcription Factors
genetics
metabolism
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Your search returned 24 results.
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21.
The role of SOX9 in autosomal sex reversal and campomelic dysplasia.
[electronic resource]
by
Schafer, A J
Dominguez-Steglich, M A
Guioli, S
Kwok, C
Weller, P A
Stevanovic, M
Weissenbach, J
Mansour, S
Young, I D
Goodfellow, P N
Producer:
19960301
In:
Philosophical transactions of the Royal Society of London. Series B, Biological sciences
vol. 350
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22.
A high-resolution whole genome radiation hybrid map of human chromosome 17q22-q25.3 across the genes for GH and TK.
[electronic resource]
by
Foster, J W
Schafer, A J
Critcher, R
Spillett, D J
Feakes, R W
Walter, M A
Dominguez-Steglich, M
Guioli, S
Brook, J D
Goodfellow, P N
Producer:
19970122
In:
Genomics
vol. 33
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23.
Dominant negative mutations in human PPARgamma associated with severe insulin resistance, diabetes mellitus and hypertension.
[electronic resource]
by
Barroso, I
Gurnell, M
Crowley, V E
Agostini, M
Schwabe, J W
Soos, M A
Maslen, G L
Williams, T D
Lewis, H
Schafer, A J
Chatterjee, V K
O'Rahilly, S
Producer:
20000110
In:
Nature
vol. 402
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24.
Familial partial lipodystrophy associated with compound heterozygosity for novel mutations in the LMNA gene.
[electronic resource]
by
Savage, D B
Soos, M A
Powlson, A
O'Rahilly, S
McFarlane, I
Halsall, D J
Barroso, I
Thomas, E L
Bell, J D
Scobie, I
Belchetz, P E
Kelly, W F
Schafer, A J
Producer:
20050110
In:
Diabetologia
vol. 47
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