Results
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Haemophilia A: database of nucleotide substitutions, deletions, insertions and rearrangements of the factor VIII gene, second edition. [electronic resource] by
- Tuddenham, E G
- Schwaab, R
- Seehafer, J
- Millar, D S
- Gitschier, J
- Higuchi, M
- Bidichandani, S
- Connor, J M
- Hoyer, L W
- Yoshioka, A
Producer: 19950103
In:
Nucleic acids research vol. 22
Availability: No items available.
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168.
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Haemophilia A: database of nucleotide substitutions, deletions, insertions and rearrangements of the factor VIII gene, second edition. [electronic resource] by
- Tuddenham, E G
- Schwaab, R
- Seehafer, J
- Millar, D S
- Gitschier, J
- Higuchi, M
- Bidichandani, S
- Connor, J M
- Hoyer, L W
- Yoshioka, A
Producer: 19941108
In:
Nucleic acids research vol. 22
Availability: No items available.
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169.
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170.
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1.4 Mb candidate gene region for X linked dyskeratosis congenita defined by combined haplotype and X chromosome inactivation analysis. [electronic resource] by
- Knight, S W
- Vulliamy, T J
- Heiss, N S
- Matthijs, G
- Devriendt, K
- Connor, J M
- D'Urso, M
- Poustka, A
- Mason, P J
- Dokal, I
Producer: 19990322
In:
Journal of medical genetics vol. 35
Availability: No items available.
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171.
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172.
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Genetic heterogeneity in tuberous sclerosis. Study of a large collaborative dataset. [electronic resource] by
- Haines, J L
- Amos, J
- Attwood, J
- Bech-Hansen, N T
- Burley, M
- Conneally, P M
- Connor, J M
- Fahsold, R
- Flodman, P
- Fryer, A
Producer: 19910702
In:
Annals of the New York Academy of Sciences vol. 615
Availability: No items available.
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173.
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174.
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175.
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176.
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A YAC contig in Xp21 containing the adrenal hypoplasia congenita and glycerol kinase deficiency genes. [electronic resource] by
- Walker, A P
- Chelly, J
- Love, D R
- Brush, Y I
- Récan, D
- Chaussain, J L
- Oley, C A
- Connor, J M
- Yates, J
- Price, D A
Producer: 19930603
In:
Human molecular genetics vol. 1
Availability: No items available.
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177.
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178.
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Genotype prediction in the fragile X syndrome. [electronic resource] by
- Hirst, M C
- Nakahori, Y
- Knight, S J
- Schwartz, C
- Thibodeau, S N
- Roche, A
- Flint, T J
- Connor, J M
- Fryns, J P
- Davies, K E
Producer: 19920204
In:
Journal of medical genetics vol. 28
Availability: No items available.
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179.
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Analysis of Scottish Duchenne and Becker muscular dystrophy families with dystrophin cDNA probes. [electronic resource] by
- Cooke, A
- Lanyon, W G
- Wilcox, D E
- Dornan, E S
- Kataki, A
- Gillard, E F
- McWhinnie, A J
- Morris, A
- Ferguson-Smith, M A
- Connor, J M
Producer: 19900717
In:
Journal of medical genetics vol. 27
Availability: No items available.
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180.
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Evidence for a familial pregnancy-induced hypertension locus in the eNOS-gene region. [electronic resource] by
- Arngrímsson, R
- Hayward, C
- Nadaud, S
- Baldursdóttir, A
- Walker, J J
- Liston, W A
- Bjarnadóttir, R I
- Brock, D J
- Geirsson, R T
- Connor, J M
- Soubrier, F
Producer: 19971015
In:
American journal of human genetics vol. 61
Availability: No items available.
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