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Journal Article
Gut, ISSN 0017-5749, 12/2017, Volume 66, Issue 12, pp. 2195 - 2196
Journal Article
Transfusion Medicine, ISSN 0958-7578, 2014, Volume 24, Issue 2, pp. 120 - 122
Journal Article
Transfusion Medicine and Hemotherapy, ISSN 1660-3796, 05/2018, Volume 45, Issue 3, pp. 173 - 177
Background: Molecular bases of blood group systems, including Rh blood group, have been poorly studied in the Indian population so far, while specificities of... 
Research Article | Allele | Phenotype | Molecular basis | D-negative | RHD
Journal Article
TRANSFUSION MEDICINE AND HEMOTHERAPY, ISSN 1660-3796, 2018, Volume 45, Issue 3, pp. 173 - 177
Background: Molecular bases of blood group systems, including Rh blood group, have been poorly studied in the Indian population so far, while specificities of... 
POPULATION | GENETIC-BASIS | Molecular basis | VARIANTS | PHENOTYPES | CHINESE | IMMUNOLOGY | GROUP SYSTEM | D-negative | RHD | WEAK-D | Allele | Phenotype | SEROLOGICALLY D | BRAZILIAN BLOOD-DONORS | HEMATOLOGY | MOLECULAR-BASIS
Journal Article
Journal of Cystic Fibrosis, ISSN 1569-1993, 2011, Volume 10, Issue 3, pp. 212 - 216
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 05/2018, Volume 102, Issue 5, pp. 832 - 844
Journal Article
Journal of Medical Genetics, ISSN 0022-2593, 11/2009, Volume 46, Issue 11, pp. 752 - 758
Journal Article
by Cogné, Benjamin and Ehresmann, Sophie and Beauregard-Lacroix, Eliane and Rousseau, Justine and Besnard, Thomas and Garcia, Thomas and Petrovski, Slavé and Avni, Shiri and McWalter, Kirsty and Blackburn, Patrick R and Sanders, Stephan J and Uguen, Kévin and Harris, Jacqueline and Cohen, Julie S and Blyth, Moira and Lehman, Anna and Berg, Jonathan and Li, Mindy H and Kini, Usha and Joss, Shelagh and von der Lippe, Charlotte and Gordon, Christopher T and Humberson, Jennifer B and Robak, Laurie and Scott, Daryl A and Sutton, Vernon R and Skraban, Cara M and Johnston, Jennifer J and Poduri, Annapurna and Nordenskjöld, Magnus and Shashi, Vandana and Gerkes, Erica H and Bongers, Ernie M.H.F and Gilissen, Christian and Zarate, Yuri A and Kvarnung, Malin and Lally, Kevin P and Kulch, Peggy A and Daniels, Brina and Hernandez-Garcia, Andres and Stong, Nicholas and McGaughran, Julie and Retterer, Kyle and Tveten, Kristian and Sullivan, Jennifer and Geisheker, Madeleine R and Stray-Pedersen, Asbjorg and Tarpinian, Jennifer M and Klee, Eric W and Sapp, Julie C and Zyskind, Jacob and Holla, Øystein L and Bedoukian, Emma and Filippini, Francesca and Guimier, Anne and Picard, Arnaud and Busk, Øyvind L and Punetha, Jaya and Pfundt, Rolph and Lindstrand, Anna and Nordgren, Ann and Kalb, Fayth and Desai, Megha and Ebanks, Ashley Harmon and Jhangiani, Shalini N and Dewan, Tammie and Coban Akdemir, Zeynep H and Telegrafi, Aida and Zackai, Elaine H and Begtrup, Amber and Song, Xiaofei and Toutain, Annick and Wentzensen, Ingrid M and Odent, Sylvie and Bonneau, Dominique and Latypova, Xénia and Deb, Wallid and Redon, Sylvia and Redon, Richard and Bilan, Frédéric and Legendre, Marine and Troyer, Caitlin and Whitlock, Kerri and Caluseriu, Oana and Murphree, Marine I and Pichurin, Pavel N and Agre, Katherine and Gavrilova, Ralitza and Rinne, Tuula and Park, Meredith and Shain, Catherine and Heinzen, Erin L and Xiao, Rui and Amiel, Jeanne and Lyonnet, Stanislas and Isidor, Bertrand and Biesecker, Leslie G and Lowenstein, Dan and Posey, Jennifer E and Denommé-Pichon, Anne-Sophie and ... and Deciphering Dev Disorders Study and CAUSES Study and Deciphering Developmental Disorders study
The American Journal of Human Genetics, ISSN 0002-9297, 03/2019, Volume 104, Issue 3, pp. 530 - 541
Journal Article
Gut, ISSN 0017-5749, 01/2009, Volume 58, Issue 1, pp. 97 - 103
Background and aims:The prevalence and natural history of hereditary pancreatitis (HP) remain poorly documented. The aims of this study were to assess genetic,... 
CATIONIC TRYPSINOGEN GENE | MEDICAL-SURGICAL SERIES | MAPS | RISK | MUTATIONS | GASTROENTEROLOGY & HEPATOLOGY