Results
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241.
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Haemophilia B: database of point mutations and short additions and deletions--second edition. [electronic resource] by
- Giannelli, F
- Green, P M
- High, K A
- Sommer, S
- Lillicrap, D P
- Ludwig, M
- Olek, K
- Reitsma, P H
- Goossens, M
- Yoshioka, A
Producer: 19910710
In:
Nucleic acids research vol. 19 Suppl
Availability: No items available.
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242.
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Expression of the alpha beta and gamma delta T-cell receptors in peripheral T-cell lymphomas. [electronic resource] by
- Gaulard, P
- Bourquelot, P
- Kanavaros, P
- Haioun, C
- Le Couedic, J P
- Divine, M
- Goossens, M
- Zafrani, E S
- Farcet, J P
- Reyes, F
Producer: 19900711
In:
Nouvelle revue francaise d'hematologie vol. 32
Availability: No items available.
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243.
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Hairy cell leukemia associated with large granular lymphocyte leukemia: immunologic and genomic study, effect of interferon treatment. [electronic resource] by
- Marolleau, J P
- Henni, T
- Gaulard, P
- Le Couedic, J P
- Gourdin, M F
- Divine, M
- Katz, A
- Tulliez, M
- Goossens, M
- Reyes, F
Producer: 19880921
In:
Blood vol. 72
Availability: No items available.
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244.
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[Antenatal diagnosis of sickle-cell anaemia by DNA analysis of amniotic fluid cells. A preliminary study in the French West-Indies (author's transl)]. [electronic resource] by
- Goossens, M
- Lee, K Y
- Dozy, A M
- Saint Martin, C
- Monplaisir, N
- Seytor, S
- Yoyo, M
- Dubart, A
- Rosa, J
- Kan, Y W
Producer: 19810613
In:
La Nouvelle presse medicale vol. 10
Availability: No items available.
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245.
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Nucleotide substitutions at the -6 position in the promoter region of the factor IX gene result in different severity of hemophilia B Leyden: consequences for genetic counseling. [electronic resource] by
- Vidaud, D
- Tartary, M
- Costa, J M
- Bahnak, B R
- Gispert-Sanchez, S
- Fressinaud, E
- Gazengel, C
- Meyer, D
- Goossens, M
- Lavergne, J M
Producer: 19930525
In:
Human genetics vol. 91
Availability: No items available.
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246.
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Haemophilia B: database of point mutations and short additions and deletions--fourth edition, 1993. [electronic resource] by
- Giannelli, F
- Green, P M
- High, K A
- Sommer, S
- Poon, M C
- Ludwig, M
- Schwaab, R
- Reitsma, P H
- Goossens, M
- Yoshioka, A
Producer: 19930817
In:
Nucleic acids research vol. 21
Availability: No items available.
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247.
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CFTR gene mutations in adults with disseminated bronchiectasis. [electronic resource] by
- Girodon, E
- Cazeneuve, C
- Lebargy, F
- Chinet, T
- Costes, B
- Ghanem, N
- Martin, J
- Lemay, S
- Scheid, P
- Housset, B
- Bignon, J
- Goossens, M
Producer: 19970930
In:
European journal of human genetics : EJHG vol. 5
Availability: No items available.
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248.
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A molecular analysis of the yemenite deaf-blind hypopigmentation syndrome: SOX10 dysfunction causes different neurocristopathies. [electronic resource] by
- Bondurand, N
- Kuhlbrodt, K
- Pingault, V
- Enderich, J
- Sajus, M
- Tommerup, N
- Warburg, M
- Hennekam, R C
- Read, A P
- Wegner, M
- Goossens, M
Producer: 20000127
In:
Human molecular genetics vol. 8
Availability: No items available.
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249.
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250.
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Haemophilia B: database of point mutations and short additions and deletions--third edition, 1992. [electronic resource] by
- Giannelli, F
- Green, P M
- High, K A
- Sommer, S
- Lillicrap, D P
- Ludwig, M
- Olek, K
- Reitsma, P H
- Goossens, M
- Yoshioka, A
Producer: 19920706
In:
Nucleic acids research vol. 20 Suppl
Availability: No items available.
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251.
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Hepatosplenic T-cell lymphoma: sinusal/sinusoidal localization of malignant cells expressing the T-cell receptor gamma delta. [electronic resource] by
- Farcet, J P
- Gaulard, P
- Marolleau, J P
- Le Couedic, J P
- Henni, T
- Gourdin, M F
- Divine, M
- Haioun, C
- Zafrani, S
- Goossens, M
Producer: 19900709
In:
Blood vol. 75
Availability: No items available.
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252.
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A single amino acid substitution in the exoplasmic domain of the human growth hormone (GH) receptor confers familial GH resistance (Laron syndrome) with positive GH-binding activity by abolishing receptor homodimerization. [electronic resource] by
- Duquesnoy, P
- Sobrier, M L
- Duriez, B
- Dastot, F
- Buchanan, C R
- Savage, M O
- Preece, M A
- Craescu, C T
- Blouquit, Y
- Goossens, M
Producer: 19940422
In:
The EMBO journal vol. 13
Availability: No items available.
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253.
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Haemophilia B: database of point mutations and short additions and deletions, fifth edition, 1994. [electronic resource] by
- Giannelli, F
- Green, P M
- Sommer, S S
- Lillicrap, D P
- Ludwig, M
- Schwaab, R
- Reitsma, P H
- Goossens, M
- Yoshioka, A
- Brownlee, G G
Producer: 19941108
In:
Nucleic acids research vol. 22
Availability: No items available.
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254.
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Polyvariant mutant cystic fibrosis transmembrane conductance regulator genes. The polymorphic (Tg)m locus explains the partial penetrance of the T5 polymorphism as a disease mutation. [electronic resource] by
- Cuppens, H
- Lin, W
- Jaspers, M
- Costes, B
- Teng, H
- Vankeerberghen, A
- Jorissen, M
- Droogmans, G
- Reynaert, I
- Goossens, M
- Nilius, B
- Cassiman, J J
Producer: 19980205
In:
The Journal of clinical investigation vol. 101
Availability: No items available.
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255.
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Haemophilia B (sixth edition): a database of point mutations and short additions and deletions. [electronic resource] by
- Giannelli, F
- Green, P M
- Sommer, S S
- Poon, M C
- Ludwig, M
- Schwaab, R
- Reitsma, P H
- Goossens, M
- Yoshioka, A
- Brownlee, G G
Producer: 19960410
In:
Nucleic acids research vol. 24
Availability: No items available.
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256.
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257.
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Haemophilia B: database of point mutations and short additions and deletions. [electronic resource] by
- Giannelli, F
- Green, P M
- High, K A
- Lozier, J N
- Lillicrap, D P
- Ludwig, M
- Olek, K
- Reitsma, P H
- Goossens, M
- Yoshioka, A
Producer: 19900906
In:
Nucleic acids research vol. 18
Availability: No items available.
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258.
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The molecular genetic analysis of hemophilia A: a directed search strategy for the detection of point mutations in the human factor VIII gene. [electronic resource] by
- Pattinson, J K
- Millar, D S
- McVey, J H
- Grundy, C B
- Wieland, K
- Mibashan, R S
- Martinowitz, U
- Tan-Un, K
- Vidaud, M
- Goossens, M
Producer: 19910129
In:
Blood vol. 76
Availability: No items available.
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259.
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DNA polymorphism of human porphobilinogen deaminase gene in acute intermittent porphyria. [electronic resource] by
- Llewellyn, D H
- Elder, G H
- Kalsheker, N A
- Marsh, O W
- Harrison, P R
- Grandchamp, B
- Picat, C
- Nordmann, Y
- Romeo, P H
- Goossens, M
Producer: 19871105
In:
Lancet (London, England) vol. 2
Availability: No items available.
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260.
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