Evidence for a gene conversion in a Hb Arya Carrier [ codon 47 Asp>Asn, Hb A1(or Hb A2):c.142 G>A]

Authors: Pcriaux, A., Paillard, C., Galoisy, A., Riou, J., Le metayer, N., Wajcman, H., Pissard, S.

Source: INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY. 39(3):e55-e59

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCRN384695137&indx=1&recIds=ETOCRN384695137

Confirmation of a founder effect in a Northern European population of a new β-globin variant: HBB:c.23_26dup (codons 8/9 (+AGAA))

Authors: Marchi, N., Pissard, S., Cliquennois, M., Vasseur, C., Le Metayer, N., Mereau, C., Jouet, J. P., Georgel, A. F., Genin, E., Rose, C.

Source: EUROPEAN JOURNAL OF HUMAN GENETICS. 23(9):1158-1164

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCRN371332611&indx=1&recIds=ETOCRN371332611

p53 gene mutations are associated with poor survival in low and low-intermediate risk diffuse large B-cell lymphomas

Authors: Leroy, K., Haioun, C., Lepage, E., Le Metayer, N., Berger, F., Labouyrie, E., Meignin, V., Petit, B., Bastard, C., Salles, G.

Source: ANNALS OF ONCOLOGY. 13(7):1108-1115

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCRN116365923&indx=1&recIds=ETOCRN116365923

This result is not displayed to guests.
Login for full access.

Evidence for a gene conversion in a Hb Arya Carrier [α codon 47 Asp>Asn, Hb A1(or Hb A2):c.142 G>A].

Authors: Pécriaux, A., Paillard, C., Galoisy, A., Riou, J., Le metayer, N., Wajcman, H., Pissard, S.

Source: International Journal of Laboratory Hematology; Jun2017, Vol. 39 Issue 3, pe55-e59, 5p

Subject Terms: JAUNDICE diagnosis, DNA analysis, AGAR, ALLELES, ELECTROPHORESIS, GENE expression, GENETIC polymorphisms, HEMOGLOBINS, JAUNDICE, LIQUID chromatography, GENETIC mutation, GENETIC testing, SEQUENCE analysis, CHILDREN

A novel ( epsilon gamma delta beta )^0-thalassemia deletion associated with an alpha globin gene triplication leading to a severe transfusion dependant fotal thalassemic syndrome

Authors: Rose, C., Rossignol, J., Lambilliotte, A., Depret, S., Le Metayer, N., Pissard, S.

Source: HAEMATOLOGICA -PAVIA THEN ROMA-. 94(4):593-593

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCRN248894294&indx=1&recIds=ETOCRN248894294

This result is not displayed to guests.
Login for full access.