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X-linked spastic paraplegia (SPG1), MASA syndrome and X-linked hydrocephalus result from mutations in the L1 gene. [electronic resource] by
- Jouet, M
- Rosenthal, A
- Armstrong, G
- MacFarlane, J
- Stevenson, R
- Paterson, J
- Metzenberg, A
- Ionasescu, V
- Temple, K
- Kenwrick, S
Producer: 19941117
In:
Nature genetics vol. 7
Availability: No items available.
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14.
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The neural cell adhesion molecule L1: genomic organisation and differential splicing is conserved between man and the pufferfish Fugu. [electronic resource] by
- Coutelle, O
- Nyakatura, G
- Taudien, S
- Elgar, G
- Brenner, S
- Platzer, M
- Drescher, B
- Jouet, M
- Kenwrick, S
- Rosenthal, A
Producer: 19980326
In:
Gene vol. 208
Availability: No items available.
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15.
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X-inactivation and marker studies in three families with incontinentia pigmenti: implications for counselling and gene localisation. [electronic resource] by
- Woffendin, H
- Jakins, T
- Jouet, M
- Stewart, H
- Landy, S
- Haan, E
- Harris, A
- Donnai, D
- Read, A
- Kenwrick, S
Producer: 19990519
In:
Clinical genetics vol. 55
Availability: No items available.
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Linkage analysis in 16 families with incontinentia pigmenti. [electronic resource] by
- Jouet, M
- Stewart, H
- Landy, S
- Yates, J
- Yong, S L
- Harris, A
- Garret, C
- Hatchwell, E
- Read, A
- Donnai, D
- Kenwrick, S
Producer: 19970930
In:
European journal of human genetics : EJHG vol. 5
Availability: No items available.
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Nine novel L1 CAM mutations in families with X-linked hydrocephalus. [electronic resource] by
- MacFarlane, J R
- Du, J S
- Pepys, M E
- Ramsden, S
- Donnai, D
- Charlton, R
- Garrett, C
- Tolmie, J
- Yates, J R
- Berry, C
- Goudie, D
- Moncla, A
- Lunt, P
- Hodgson, S
- Jouet, M
- Kenwrick, S
Producer: 19970822
In:
Human mutation vol. 9
Availability: No items available.
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