Results
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Heterozygous HESX1 mutations associated with isolated congenital pituitary hypoplasia and septo-optic dysplasia by
- Thomas, P. Q
- Beddington, R. S. P
- Brickman, J. M
- Cameron, F
- Dattani, M. T
- Dunger, D
- Forrest, S
- Hurst, J
- Mcnay, D
- Robinson, I. C. A. F
- Stanhope, R
- Warne, G
- Woods, K
- Zacharin, M
Material type: Text; Format:
print ; Literary form:
Not fiction
In: Human Molecular Genetics 10 (1), 39-45.
Availability: Items available for loan: Staff publications (1)Call number: XX(11037.1).
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Recombinational DNA double-strand breaks in mice precede synapsis by
- Mahadevaiah, S. K
- Baudat, F
- Blanco-Rodriguez, J
- Bonner, W. M
- Burgoyne, P. S
- De Boer, P
- Jasin, M
- Keeney, S
- Rogakou, E. P
- Turner, J. M. A
Material type: Text; Format:
print ; Literary form:
Not fiction
In: Nature Genetics 27 (3), 271-276.
Availability: Items available for loan: Staff publications (1)Call number: XX(11080.1).
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Spectrum of dominant mutations in the desmosomal cadherin desmoglein 1, causing the skin disease striate palmoplantar keratoderma by
- Hunt, D. M
- Armstrong, D. K. B
- Arnemann, J
- Buxton, R. S
- Dopping-Hepenstal, P. J. C
- Eady, R. A
- Hennies, H. C
- Hughes, A. E
- Kelsell, D. P
- Kuster, W
- Leigh, I. M
- McGrath, J. A
- Rickman, L
- Simrak, D
- Stevens, H. P
- Whittock, N. V
Material type: Text; Format:
print ; Literary form:
Not fiction
In: European Journal of Human Genetics 9 (3), 197-203.
Availability: Items available for loan: Staff publications (1)Call number: XX(11098.1).
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A Y-encoded subunit of the translation initiation factor Eif2 is essential for mouse spermatogenesis by
- Mazeyrat, S
- Bishop, C
- Burgoyne, P. S
- Eicher, E. M
- Grigoriev, V
- Mahadevaiah, S. K
- Mitchell, M. J
- Ojarikre, O. A
- Rattigan, A
- Saut, N
Material type: Text; Format:
print ; Literary form:
Not fiction
In: Nature Genetics 29 (1), 49-53.
Availability: Items available for loan: Staff publications (1)Call number: XX(11211.1).
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