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Germline deletion in a neurofibromatosis type 2 kindred inactivates the NF2 gene and a candidate meningioma locus. [electronic resource] by
- Sanson, M
- Marineau, C
- Desmaze, C
- Lutchman, M
- Ruttledge, M
- Baron, C
- Narod, S
- Delattre, O
- Lenoir, G
- Thomas, G
Producer: 19931105
In:
Human molecular genetics vol. 2
Availability: No items available.
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Evidence for the complete inactivation of the NF2 gene in the majority of sporadic meningiomas. [electronic resource] by
- Ruttledge, M H
- Sarrazin, J
- Rangaratnam, S
- Phelan, C M
- Twist, E
- Merel, P
- Delattre, O
- Thomas, G
- Nordenskjöld, M
- Collins, V P
Producer: 19940525
In:
Nature genetics vol. 6
Availability: No items available.
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12.
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Physical mapping of the NF2/meningioma region on human chromosome 22q12. [electronic resource] by
- Ruttledge, M H
- Xie, Y G
- Han, F Y
- Giovannini, M
- Janson, M
- Fransson, I
- Werelius, B
- Delattre, O
- Thomas, G
- Evans, G
Producer: 19940621
In:
Genomics vol. 19
Availability: No items available.
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13.
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Neurofibromatosis type 2 appears to be a genetically homogeneous disease. [electronic resource] by
- Narod, S A
- Parry, D M
- Parboosingh, J
- Lenoir, G M
- Ruttledge, M
- Fischer, G
- Eldridge, R
- Martuza, R L
- Frontali, M
- Haines, J
Producer: 19920910
In:
American journal of human genetics vol. 51
Availability: No items available.
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Cloning of a novel, anonymous gene from a megabase-range YAC and cosmid contig in the neurofibromatosis type 2/meningioma region on human chromosome 22q12. [electronic resource] by
- Xie, Y G
- Han, F Y
- Peyrard, M
- Ruttledge, M H
- Fransson, I
- DeJong, P
- Collins, J
- Dunham, I
- Nordenskjöld, M
- Dumanski, J P
Producer: 19931230
In:
Human molecular genetics vol. 2
Availability: No items available.
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Characterization of a new member of the human beta-adaptin gene family from chromosome 22q12, a candidate meningioma gene. [electronic resource] by
- Peyrard, M
- Fransson, I
- Xie, Y G
- Han, F Y
- Ruttledge, M H
- Swahn, S
- Collins, J E
- Dunham, I
- Collins, V P
- Dumanski, J P
Producer: 19950110
In:
Human molecular genetics vol. 3
Availability: No items available.
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16.
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Presymptomatic diagnosis for neurofibromatosis 2 with chromosome 22 markers. [electronic resource] by
- Ruttledge, M H
- Narod, S A
- Dumanski, J P
- Parry, D M
- Eldridge, R
- Wertelecki, W
- Parboosingh, J
- Faucher, M C
- Lenoir, G M
- Collins, V P
Producer: 19931025
In:
Neurology vol. 43
Availability: No items available.
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17.
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Machado Joseph disease maps to the same region of chromosome 14 as the spinocerebellar ataxia type 3 locus. [electronic resource] by
- Twist, E C
- Casaubon, L K
- Ruttledge, M H
- Rao, V S
- Macleod, P M
- Radvany, J
- Zhao, Z
- Rosenberg, R N
- Farrer, L A
- Rouleau, G A
Producer: 19950427
In:
Journal of medical genetics vol. 32
Availability: No items available.
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18.
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The human mammary-derived growth inhibitor (MDGI) gene: genomic structure and mutation analysis in human breast tumors. [electronic resource] by
- Phelan, C M
- Larsson, C
- Baird, S
- Futreal, P A
- Ruttledge, M H
- Morgan, K
- Tonin, P
- Hung, H
- Korneluk, R G
- Pollak, M N
- Narod, S A
Producer: 19961213
In:
Genomics vol. 34
Availability: No items available.
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19.
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Ovarian cancer risk in BRCA1 carriers is modified by the HRAS1 variable number of tandem repeat (VNTR) locus. [electronic resource] by
- Phelan, C M
- Rebbeck, T R
- Weber, B L
- Devilee, P
- Ruttledge, M H
- Lynch, H T
- Lenoir, G M
- Stratton, M R
- Easton, D F
- Ponder, B A
- Cannon-Albright, L
- Larsson, C
- Goldgar, D E
- Narod, S A
Producer: 19960325
In:
Nature genetics vol. 12
Availability: No items available.
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20.
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Type of mutation in the neurofibromatosis type 2 gene (NF2) frequently determines severity of disease. [electronic resource] by
- Ruttledge, M H
- Andermann, A A
- Phelan, C M
- Claudio, J O
- Han, F Y
- Chretien, N
- Rangaratnam, S
- MacCollin, M
- Short, P
- Parry, D
- Michels, V
- Riccardi, V M
- Weksberg, R
- Kitamura, K
- Bradburn, J M
- Hall, B D
- Propping, P
- Rouleau, G A
Producer: 19960925
In:
American journal of human genetics vol. 59
Availability: No items available.
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