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Diagnosis and management challenges in patients with mild haemophilia A and discrepant FVIII measurements. [electronic resource] by
- Trossaert, M
- Lienhart, A
- Nougier, C
- Fretigny, M
- Sigaud, M
- Meunier, S
- Fouassier, M
- Ternisien, C
- Negrier, C
- Dargaud, Y
Producer: 20150209
In:
Haemophilia : the official journal of the World Federation of Hemophilia vol. 20
Availability: No items available.
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15.
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Study of six patients with complete F9 deletion characterized by cytogenetic microarray: role of the SOX3 gene in intellectual disability. [electronic resource] by
- Jourdy, Y
- Chatron, N
- Carage, M-L
- Fretigny, M
- Meunier, S
- Zawadzki, C
- Gay, V
- Negrier, C
- Sanlaville, D
- Vinciguerra, C
Producer: 20171227
In:
Journal of thrombosis and haemostasis : JTH vol. 14
Availability: No items available.
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16.
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Molecular cytogenetic characterization of five F8 complex rearrangements: utility for haemophilia A genetic counselling. [electronic resource] by
- Jourdy, Y
- Chatron, N
- Fretigny, M
- Carage, M L
- Chambost, H
- Claeyssens-Donadel, S
- Roussel-Robert, V
- Negrier, C
- Sanlaville, D
- Vinciguerra, C
Producer: 20180319
In:
Haemophilia : the official journal of the World Federation of Hemophilia vol. 23
Availability: No items available.
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