Blood group genotyping von Westhoff, Connie M.

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Monoclonal anti‐CD47 interference in red cell and platelet testing von Velliquette, Randall W., Aeschlimann, Judith, Kirkegaard, Julie, Shakarian, Gayane, Lomas‐Francis, Christine, Westhoff, Connie M.

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Function of human Rh based on structure of RhCG at 2.1 Å von Gruswitz, Franz, Chaudhary, Sarika, Ho, Joseph D, Schlessinger, Avner, Pezeshki, Bobak, Ho, Chi-Min, Sali, Andrej, Westhoff, Connie M, Stroud, Robert M

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Intricacies of GATA-ca, Continued von Lomas-Francis, Christine, Stone, Elizabeth F, Westhoff, Connie M, Shi, Patricia A

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Ammonia secretion from fish gill depends on a set of Rh glycoproteins von Nakada, Tsutomu, Westhoff, Connie M., Kato, Akira, Hirose, Shigehisa

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How do I manage Rh typing in obstetric patients? von Haspel, Richard L., Westhoff , Connie M.

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Disruption of the tumour-associated EMP3 enhances erythroid proliferation and causes the MAM-negative phenotype von Thornton, Nicole, Karamatic Crew, Vanja, Tilley, Louise, Green, Carole A., Tay, Chwen Ling, Griffiths, Rebecca E., Singleton, Belinda K., Spring, Frances, Walser, Piers, Alattar, Abdul Ghani, Jones, Benjamin, Laundy, Rosalind, Storry, Jill R., Möller, Mattias, Wall, Lorna, Charlewood, Richard, Westhoff, Connie M., Lomas-Francis, Christine, Yahalom, Vered, Feick, Ute, Seltsam, Axel, Mayer, Beate, Olsson, Martin L., Anstee, David J.

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Severe delayed hemolytic transfusion reaction due to anti-Fy3 in a patient with sickle cell disease undergoing red cell exchange prior to hematopoietic progenitor cell collection f... von Stone, Elizabeth F, Avecilla, Scott T, Wuest, David L, Lomas-Francis, Christine, Westhoff, Connie M, Diuguid, David L, Sadelain, Michel, Boulad, Farid, Shi, Patricia A

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PIGG defines the Emm blood group system von Lane, William J., Aeschlimann, Judith, Vege, Sunitha, Lomas-Francis, Christine, Burgos, Anna, Mah, Helen H., Halls, Justin B. L., Baeck, Peter, Ligthart, Peter C., Veldhuisen, Barbera, Shah, Ripal J., Joshi, Sanmukh R., Westhoff, Connie M.

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Blood group genotype matching for transfusion von Westhoff, Connie M, Floch, Aline

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Whole-exome sequencing for RH genotyping and alloimmunization risk in children with sickle cell anemia von Chou, Stella T., Flanagan, Jonathan M., Vege, Sunitha, Luban, Naomi L.C., Brown, R. Clark, Ware, Russell E., Westhoff, Connie M.

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The protean presentations of XK disease (McLeod syndrome): a case series with new observations and updates on previously reported families von Walker, Ruth H, Barreto, Mariana, Bateman, James R, Bustamante, M Leonor, Chiu, Graham, Feitell, Scott, Frey, Beat M, Guerra, Patricio, Guerrero, Sofia, Jung, Hans H, Maldonado, Fernando, Meyer, Eduardo, Miranda, Marcelo, McFarland, Emelie, Oates, Patricia, Ochoa, Gorka, Olsson, Karin, Paucar, Martin, Proschle, Jonatan Alvarez, Sammler, Esther M, Troncoso, Monica, Wu-Wallace, Rachel, Young, Leo, Vege, Sunitha, Westhoff, Connie M, Danek, Adrian

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Erythroid transcription factor EKLF/KLF1 mutation causing congenital dyserythropoietic anemia type IV in a patient of Taiwanese origin: Review of all reported cases and development... von Jaffray, Julie A., Mitchell, W. Beau, Gnanapragasam, Merlin Nithya, Seshan, Surya V., Guo, Xinhuo, Westhoff, Connie M., Bieker, James J., Manwani, Deepa

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High prevalence of red blood cell alloimmunization in sickle cell disease despite transfusion from Rh-matched minority donors von Chou, Stella T., Jackson, Tannoa, Vege, Sunitha, Smith-Whitley, Kim, Friedman, David F., Westhoff, Connie M.

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P-Null Phenotype Due to a Rare Frame-Shift Mutation and with Allo-Anti-PP1Pk Causing a Severe Hemolytic Transfusion Reaction: A Case Report with Clinical Management von Kanani, Ashish N., Senjaliya, Snehal B., Rajapara, Manisha M., Aeschlimann, Judith, Westhoff, Connie M., Joshi, Sanmukh R.

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Anti-Emm, a rare specificity to the high-incidence antigen Emm in an Indian patient defining the new blood group system EMM (ISBT042) von Shah, Ripal J, Senjaliya, Snehal B, Harimoorthy, V, Burgos, Anna, Vege, Sunitha, Lomas-Francis, Christine, Westhoff, Connie M, Joshi, Sanmukh Ratilal

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RH genotype matching for transfusion support in sickle cell disease von Chou, Stella T., Evans, Perry, Vege, Sunitha, Coleman, Sarita L., Friedman, David F., Keller, Margaret, Westhoff, Connie M.

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Alloimmunization in patients with sickle cell disease and underrecognition of accompanying delayed hemolytic transfusion reactions von Coleman, Sarita, Westhoff, Connie M., Friedman, David F., Chou, Stella T.

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AMIS and antigen modulation: of mice and men von Westhoff, Connie M.

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Characterization of ammonia transport by the kidney Rh glycoproteins RhBG and RhCG von Mak, Don-On Daniel, Dang, Binh, Weiner, I David, Foskett, J Kevin, Westhoff, Connie M

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