المؤلفون: Hussain, S, Hosdurga, S

المصدر: Down syndrome medical interest group, british association of community child health and british paediatric respiratory society ; page A101.2-A101

الاتاحة: http://dx.doi.org/10.1136/archdischild-2020-rcpch.240
https://syndication.highwire.org/content/doi/10.1136/archdischild-2020-rcpch.240

المؤلفون: Sy, M. R., Chauhan, J., Prescott, K., Imam, A., Kraus, A., Beleza, A., Salkeld, L., Hosdurga, S., Parker, M., Vasudevan, P., Islam, L., Goel, H., Bain, N., Park, S. M., Mohammed, S., Dieterich, K., Coutton, C., Satre, V., Vieville, G., Donaldson, A., Beneteau, C., Ghoumid, Jamal, Van Den Bogaert, K., Boogaerts, A., Boudry, E., Vanlerberghe, Clemence, Petit, Florence, Bernardini, L., Torres, B., Mattina, T., Carli, D., Mandrile, G., Pinelli, M., Brunetti-Pierri, N., Neas, K., Beddow, R., Tørring, P. M., Faletra, F., Spedicati, B., Gasparini, P., Mussa, A., Ferrero, G. B., Lampe, A., Lam, W., Bi, W., Bacino, C. A., Kuwahara, A., Bush, J. O., Zhao, X., Luna, P. N., Shaw, C. A., Rosenfeld, J. A., Scott, D. A.

المساهمون: Université de Lille, CHU Lille, Maladies Rares du Développement : Génétique, Régulation et Protéomique (RADEME) - ULR 7364

مصطلحات موضوعية: esophageal atresia, exome sequencing, Fanconi anemia, NRXN1, TCF4, tracheoesophageal fistula

وصف الملف: application/octet-stream

Relation: American Journal of Medical Genetics Part A; http://hdl.handle.net/20.500.12210/84137

الاتاحة: https://hdl.handle.net/20.500.12210/84137

المؤلفون: Sy, M. R., Chauhan, J., Prescott, K., Imam, A., Kraus, A., Beleza, A., Salkeld, L., Hosdurga, S., Parker, M., Vasudevan, P., Islam, L., Goel, H., Bain, N., Park, S. M., Mohammed, S., Dieterich, K., Coutton, C., Satre, V., Vieville, G., Donaldson, A., Beneteau, C., Ghoumid, Jamal, van den Bogaert, K., Boogaerts, A., Boudry, E., Vanlerberghe, Clemence, Petit, Florence, Bernardini, L., Torres, B., Mattina, T., Carli, D., Mandrile, G., Pinelli, M., Brunetti-Pierri, N., Neas, K., Beddow, R., Tørring, P. M., Faletra, F., Spedicati, B., Gasparini, P., Mussa, A., Ferrero, G. B., Lampe, A., Lam, W., Bi, W., Bacino, C. A., Kuwahara, A., Bush, J. O., Zhao, X., Luna, P. N., Shaw, C. A., Rosenfeld, J. A., Scott, D. A.

المساهمون: Maladies RAres du DEveloppement embryonnaire et du MEtabolisme : du Phénotype au Génotype et à la Fonction - ULR 7364 (RADEME), Université de Lille-Centre Hospitalier Régional Universitaire CHU Lille (CHRU Lille)

المصدر: ISSN: 1552-4825.

مصطلحات موضوعية: esophageal atresia, exome sequencing, Fanconi anemia, NRXN1, TCF4, tracheoesophageal fistula, [SDV]Life Sciences [q-bio]

Relation: info:eu-repo/semantics/altIdentifier/pmid/36135330; hal-04193913; https://hal.univ-lille.fr/hal-04193913; PUBMED: 36135330

الاتاحة: https://hal.univ-lille.fr/hal-04193913
https://doi.org/10.1002/ajmg.a.62976

المؤلفون: Hosdurga, S, Basude, D, Spray, C, Gardner, C, Sandhu, B

مصطلحات موضوعية: British Association of General Paediatrics/British Society of Paediatric Gastroenterology, Hepatology and Nutrition

وصف الملف: text/html

Relation: http://adc.bmj.com/cgi/content/short/95/1_MeetingAbstracts/A56-a; http://dx.doi.org/10.1136/adc.2010.186338.127

الاتاحة: http://adc.bmj.com/cgi/content/short/95/1_MeetingAbstracts/A56-a
https://doi.org/10.1136/adc.2010.186338.127

المؤلفون: Amin, S., Hosdurga, S., Lux, A., Sharpies, P., Patel, J., O'Callaghan, F.

المصدر: European Journal of Paediatric Neurology; May2011 Supplement 1, Vol. 15, pS59-S59, 1p