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1. Srivannaboon, K; Conley, ME; Coustan-Smith, E; Wang, WC
   Hypogammaglobulinemia and reduced numbers of B-cells in children with myelodysplastic syndrome
   JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY
   
   K. Srivannaboon et al., "Hypogammaglobulinemia and reduced numbers of B-cells in children with myelodysplastic syndrome", J PED H ONC, 23(2), 2001, pp. 122-125
2. Minegishi, Y; Conley, ME
   Negative selection at the pre-BCR checkpoint elicited by human mu heavy chains with unusual CDR3 regions
   IMMUNITY
   
   Y. Minegishi e M.E. Conley, "Negative selection at the pre-BCR checkpoint elicited by human mu heavy chains with unusual CDR3 regions", IMMUNITY, 14(5), 2001, pp. 631-641
3. Doffinger, R; Smahi, A; Bessia, C; Geissmann, F; Feinberg, J; Durandy, A; Bodemer, C; Kenwrick, S; Dupuis-Girod, S; Blanche, S; Wood, P; Rabia, SH; Headon, DJ; Overbeek, PA; Le Deist, F; Holland, SM; Belani, K; Kumararatne, DS; Fischer, A; Shapiro, R; Conley, ME; Reimund, E; Kalhoff, H; Abinun, M; Munnich, A; Israel, A; Courtois, G; Casanova, JL
   X-linked anhidrotic ectodermal dysplasia with immunodeficiency is caused by impaired NF-kappa B signaling
   NATURE GENETICS
   
   R. Doffinger et al., "X-linked anhidrotic ectodermal dysplasia with immunodeficiency is caused by impaired NF-kappa B signaling", NAT GENET, 27(3), 2001, pp. 277-285
4. Richter, D; Conley, ME; Rohrer, J; Myers, LA; Zahradka, K; Kelecic, J; Sertic, J; Stavljenic-Rukavina, A
   A contiguous deletion syndrome of X-linked agammaglobulinemia and sensorineural deafness
   PEDIATRIC ALLERGY AND IMMUNOLOGY
   
   D. Richter et al., "A contiguous deletion syndrome of X-linked agammaglobulinemia and sensorineural deafness", PEDIAT A IM, 12(2), 2001, pp. 107-111
5. Wang, DM; Boylin, EC; Minegishi, Y; Wen, RR; Smith, CIE; Ihle, JN; Conley, ME
   Variations in the human phospholipase C gamma 2 gene in patients with B-cell defects of unknown etiology
   IMMUNOGENETICS
   
   D.M. Wang et al., "Variations in the human phospholipase C gamma 2 gene in patients with B-cell defects of unknown etiology", IMMUNOGENET, 53(7), 2001, pp. 550-556
6. Villa, A; Sobacchi, C; Notarangelo, LD; Bozzi, F; Abinun, M; Abrahamsen, TG; Arkwright, PD; Baniyash, M; Brooks, EG; Conley, ME; Cortes, P; Duse, M; Fasth, A; Filipovich, AM; Infante, AJ; Jones, A; Mazzolari, E; Muller, SM; Pasic, S; Rechavi, G; Sacco, MG; Santagata, S; Schroeder, ML; Seger, R; Strina, D; Ugazio, A; Valiaho, J; Vihinen, M; Vogler, LB; Ochs, H; Vezzoni, P; Friedrich, W; Schwarz, K
   V(D)J recombination defects in lymphocytes due to RAG mutations: severe immunodeficiency with a spectrum of clinical presentations
   BLOOD
   
   A. Villa et al., "V(D)J recombination defects in lymphocytes due to RAG mutations: severe immunodeficiency with a spectrum of clinical presentations", BLOOD, 97(1), 2001, pp. 81-88
7. Minegishi, Y; Lavoie, A; Cunningham-Rundles, C; Bedard, PM; Hebert, J; Cote, L; Dan, K; Sedlak, D; Buckley, RH; Fischer, A; Durandy, A; Conley, ME
   Mutations in activation-induced cytidine deaminase in patients with hyper IgM syndrome
   CLINICAL IMMUNOLOGY
   
   Y. Minegishi et al., "Mutations in activation-induced cytidine deaminase in patients with hyper IgM syndrome", CLIN IMMUNO, 97(3), 2000, pp. 203-210
8. Conley, ME; Rohrer, J; Minegishi, Y
   X-linked agammaglobulinemia
   CLINICAL REVIEWS IN ALLERGY & IMMUNOLOGY
   
   M.E. Conley et al., "X-linked agammaglobulinemia", CL R ALL IM, 19(2), 2000, pp. 183-204
9. Slobod, KS; Sandlund, JT; Spiegel, PH; Haik, B; Hurwitz, JL; Conley, ME; Bowman, LC; Benaim, E; Jenkins, JJ; Stocks, RMS; Gan, YJ; Sixbey, JW
   Molecular evidence of ocular Epstein-Barr virus infection
   CLINICAL INFECTIOUS DISEASES
   
   K.S. Slobod et al., "Molecular evidence of ocular Epstein-Barr virus infection", CLIN INF D, 31(1), 2000, pp. 184-188
10. Conley, ME; Rohrer, J; Rapalus, L; Boylin, EC; Minegishi, Y
    Defects in early B-cell development: comparing the consequences of abnormalities in pre-BCR signaling in the human and the mouse
    IMMUNOLOGICAL REVIEWS
    
    M.E. Conley et al., "Defects in early B-cell development: comparing the consequences of abnormalities in pre-BCR signaling in the human and the mouse", IMMUNOL REV, 178, 2000, pp. 75-90
11. Webb, CF; Yamashita, Y; Ayers, N; Evetts, S; Paulin, Y; Conley, ME; Smith, EA
    The transcription factor Bright associates with Bruton's tyrosine kinase, the defective protein in immunodeficiency disease
    JOURNAL OF IMMUNOLOGY
    
    C.F. Webb et al., "The transcription factor Bright associates with Bruton's tyrosine kinase, the defective protein in immunodeficiency disease", J IMMUNOL, 165(12), 2000, pp. 6956-6965
12. Gaspar, HB; Conley, ME
    Early B cell defects
    CLINICAL AND EXPERIMENTAL IMMUNOLOGY
    
    H.B. Gaspar e M.E. Conley, "Early B cell defects", CLIN EXP IM, 119(3), 2000, pp. 383-389
13. Hiel, JA; Weemaes, CM; van den Heuvel, LP; van Engelen, BG; Gabreels, FJ; Smeets, DF; van der Burgt, I; Chrzanovska, KH; Bernatowska, E; Krajewska-Walasek, M; Bialecka, M; Abramczuk, D; Gregorek, H; Michalkiewicz, I; Perek, D; Midro, AT; Seemanova, E; Belohradsky, BH; Solder, B; Barbi, G; Wegner, RD; Sperling, K; Dixon, J; Maraschio, P; Marseglia, GL; Green, A; Taylor, AM; Der Kaloustian, VM; Komatsu, K; Matsuura, S; Conley, ME; Concannon, P; Gatti, RA
    Nijmegen breakage syndrome
    ARCHIVES OF DISEASE IN CHILDHOOD
    
    J.A. Hiel et al., "Nijmegen breakage syndrome", ARCH DIS CH, 82(5), 2000, pp. 400-406
14. Conley, ME
    Diagnostic guidelines - An international consensus document
    CLINICAL IMMUNOLOGY
    
    M.E. Conley, "Diagnostic guidelines - An international consensus document", CLIN IMMUNO, 93(3), 1999, pp. 189-189
15. Conley, ME; Notarangelo, LD; Etzioni, A
    Diagnostic criteria for primary immunodeficiencies
    CLINICAL IMMUNOLOGY
    
    M.E. Conley et al., "Diagnostic criteria for primary immunodeficiencies", CLIN IMMUNO, 93(3), 1999, pp. 190-197
16. Conley, ME; Rapalus, L; Boylin, EC; Rohrer, J; Minegishi, Y
    Gene conversion events contribute to the polymorphic variation of the surrogate light chain gene lambda 5/14.1
    CLINICAL IMMUNOLOGY
    
    M.E. Conley et al., "Gene conversion events contribute to the polymorphic variation of the surrogate light chain gene lambda 5/14.1", CLIN IMMUNO, 93(2), 1999, pp. 162-167
17. Rohrer, J; Minegishi, Y; Richter, D; Eguiguren, J; Conley, ME
    Unusual mutations in Btk: An insertion, a duplication, an inversion, and four large deletions
    CLINICAL IMMUNOLOGY
    
    J. Rohrer et al., "Unusual mutations in Btk: An insertion, a duplication, an inversion, and four large deletions", CLIN IMMUNO, 90(1), 1999, pp. 28-37
18. Vihinen, M; Kwan, SP; Lester, T; Ochs, HD; Resnick, I; Valiaho, J; Conley, ME; Smith, CIE
    Mutations of the human BTK gene coding for Bruton tyrosine kinase in X-linked agammaglobulinemia
    HUMAN MUTATION
    
    M. Vihinen et al., "Mutations of the human BTK gene coding for Bruton tyrosine kinase in X-linked agammaglobulinemia", HUM MUTAT, 13(4), 1999, pp. 280-285
19. Conley, ME
    Genetic effects on immunity - New genes - how do they fit? Editorial overview
    CURRENT OPINION IN IMMUNOLOGY
    
    M.E. Conley, "Genetic effects on immunity - New genes - how do they fit? Editorial overview", CURR OP IM, 11(4), 1999, pp. 427-430
20. Minegishi, Y; Rohrer, J; Coustan-Smith, E; Lederman, HM; Pappu, R; Campana, D; Chan, AC; Conley, ME
    An essential role for BLNK in human B cell development
    SCIENCE
    
    Y. Minegishi et al., "An essential role for BLNK in human B cell development", SCIENCE, 286(5446), 1999, pp. 1954-1957
21. Minegishi, Y; Hendershot, LM; Conley, ME
    Novel mechanisms control the folding and assembly of lambda 5/14.1 and VpreB to produce an intact surrogate light chain
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    
    Y. Minegishi et al., "Novel mechanisms control the folding and assembly of lambda 5/14.1 and VpreB to produce an intact surrogate light chain", P NAS US, 96(6), 1999, pp. 3041-3046
22. Minegishi, Y; Coustan-Smith, E; Rapalus, L; Ersoy, F; Campana, D; Conley, ME
    Mutations in Ig alpha (CD79a) result in in B-cell development
    JOURNAL OF CLINICAL INVESTIGATION
    
    Y. Minegishi et al., "Mutations in Ig alpha (CD79a) result in in B-cell development", J CLIN INV, 104(8), 1999, pp. 1115-1121
23. Rohrer, J; Conley, ME
    Correction of X-linked immunodeficient mice by competitive reconstitution with limiting numbers of normal bone marrow cells
    BLOOD
    
    J. Rohrer e M.E. Conley, "Correction of X-linked immunodeficient mice by competitive reconstitution with limiting numbers of normal bone marrow cells", BLOOD, 94(10), 1999, pp. 3358-3365
24. CONLEY ME; COOPER MD
    GENETIC-BASIS OF ABNORMAL B-CELL DEVELOPMENT
    Current opinion in immunology
    
    M.E. Conley e M.D. Cooper, "GENETIC-BASIS OF ABNORMAL B-CELL DEVELOPMENT", Current opinion in immunology, 10(4), 1998, pp. 399-406
25. MINEGISHI Y; CONLEY ME
    FAILURE OF IMMUNOGLOBULIN LIGHT-CHAIN REARRANGEMENT TO RESCUE B-CELL DEVELOPMENT IN A PATIENT WITH LAMBDA-5 14.1 DEFICIENCY/
    The FASEB journal
    
    Y. Minegishi e M.E. Conley, "FAILURE OF IMMUNOGLOBULIN LIGHT-CHAIN REARRANGEMENT TO RESCUE B-CELL DEVELOPMENT IN A PATIENT WITH LAMBDA-5 14.1 DEFICIENCY/", The FASEB journal, 12(5), 1998, pp. 5339-5339
26. ROHRER J; CONLEY ME
    CORRECTION OF BTK DEFICIENT MICE BY COMPETITIVE REPOPULATION OF BONE-MARROW CELLS
    The FASEB journal
    
    J. Rohrer e M.E. Conley, "CORRECTION OF BTK DEFICIENT MICE BY COMPETITIVE REPOPULATION OF BONE-MARROW CELLS", The FASEB journal, 12(5), 1998, pp. 5341-5341
27. CONLEY ME
    GENETIC-COUNSELING FOR PRIMARY IMMUNODEFICIENCIES
    Molecular immunology
    
    M.E. Conley, "GENETIC-COUNSELING FOR PRIMARY IMMUNODEFICIENCIES", Molecular immunology, 35(11-12), 1998, pp. 629-630
28. YEL L; CONLEY ME; HERROD HG
    IMMUNOLOGICAL FINDINGS IN INFANTS WITH WISKOTT-ALDRICH-SYNDROME
    Journal of allergy and clinical immunology
    
    L. Yel et al., "IMMUNOLOGICAL FINDINGS IN INFANTS WITH WISKOTT-ALDRICH-SYNDROME", Journal of allergy and clinical immunology, 101(1), 1998, pp. 297-297
29. MINEGISHI Y; COUSTANSMITH E; WANG YH; COOPER MD; CAMPANA D; CONLEY ME
    MUTATIONS IN THE HUMAN LAMBDA-5 14.1 GENE RESULT IN B-CELL DEFICIENCYAND AGAMMAGLOBULINEMIA/
    The Journal of experimental medicine
    
    Y. Minegishi et al., "MUTATIONS IN THE HUMAN LAMBDA-5 14.1 GENE RESULT IN B-CELL DEFICIENCYAND AGAMMAGLOBULINEMIA/", The Journal of experimental medicine, 187(1), 1998, pp. 71-77
30. KITANAKA A; MANO H; CONLEY ME; CAMPANA D
    EXPRESSION AND ACTIVATION OF THE NONRECEPTOR TYROSINE KINASE TEC IN HUMAN B-CELLS
    Blood
    
    A. Kitanaka et al., "EXPRESSION AND ACTIVATION OF THE NONRECEPTOR TYROSINE KINASE TEC IN HUMAN B-CELLS", Blood, 91(3), 1998, pp. 940-948
31. ROHRER J; CONLEY ME
    TRANSCRIPTIONAL REGULATORY ELEMENTS WITHIN THE FIRST INTRON OF BRUTONS TYROSINE KINASE
    Blood
    
    J. Rohrer e M.E. Conley, "TRANSCRIPTIONAL REGULATORY ELEMENTS WITHIN THE FIRST INTRON OF BRUTONS TYROSINE KINASE", Blood, 91(1), 1998, pp. 214-221
32. CONLEY ME; MATHIAS D; TREADAWAY J; MINEGISHI Y; ROHRER J
    MUTATIONS IN BTK IN PATIENTS WITH PRESUMED X-LINKED AGAMMAGLOBULINEMIA
    American journal of human genetics
    
    M.E. Conley et al., "MUTATIONS IN BTK IN PATIENTS WITH PRESUMED X-LINKED AGAMMAGLOBULINEMIA", American journal of human genetics, 62(5), 1998, pp. 1034-1043
33. YEL L; TRUBEL H; BUCKLEY RH; PACHMAN LM; CONLEY ME
    CLINICAL-FEATURES IN PATIENTS WITH MUTATIONS IN THE IMMUNOGLOBULIN-MUHEAVY-CHAIN GENE
    Journal of allergy and clinical immunology
    
    L. Yel et al., "CLINICAL-FEATURES IN PATIENTS WITH MUTATIONS IN THE IMMUNOGLOBULIN-MUHEAVY-CHAIN GENE", Journal of allergy and clinical immunology, 99(1), 1997, pp. 1927-1927
34. ROHRER J; CONLEY ME
    TRANSCRIPTION CONTROL ELEMENTS IN THE FIRST INTRON OF BTK
    Journal of allergy and clinical immunology
    
    J. Rohrer e M.E. Conley, "TRANSCRIPTION CONTROL ELEMENTS IN THE FIRST INTRON OF BTK", Journal of allergy and clinical immunology, 99(1), 1997, pp. 1928-1928
35. CONLEY ME
    AN EVOLVING VIEW OF HYPER-IGM SYNDROME
    The Journal of pediatrics
    
    M.E. Conley, "AN EVOLVING VIEW OF HYPER-IGM SYNDROME", The Journal of pediatrics, 131(1), 1997, pp. 8-9
36. KITANAKA A; MANO H; CONLEY ME; CAMPANA D
    EXPRESSION AND ACTIVATION OF THE NONRECEPTOR TYROSINE KINASE TEC IN HUMAN B-CELLS
    Blood
    
    A. Kitanaka et al., "EXPRESSION AND ACTIVATION OF THE NONRECEPTOR TYROSINE KINASE TEC IN HUMAN B-CELLS", Blood, 90(10), 1997, pp. 80-80
37. PUCK JM; PEPPER AE; HENTHORN PS; CANDOTTI F; ISAKOV J; WHITWAM T; CONLEY ME; FISCHER RE; ROSENBLATT HM; SMALL TN; BUCKLEY RH
    MUTATION ANALYSIS OF IL2RG IN HUMAN X-LINKED SEVERE COMBINED IMMUNODEFICIENCY
    Blood
    
    J.M. Puck et al., "MUTATION ANALYSIS OF IL2RG IN HUMAN X-LINKED SEVERE COMBINED IMMUNODEFICIENCY", Blood, 89(6), 1997, pp. 1968-1977
38. GROSS TG; FILIPOVICH AH; CONLEY ME; PRACHER E; SCHMIEGELOW K; VERDIRAME JD; VOWELS M; WILLIAMS LL; SEEMAYER TA
    CURE OF X-LINKED LYMPHOPROLIFERATIVE DISEASE (XLP) WITH ALLOGENEIC HEMATOPOIETIC STEM-CELL TRANSPLANTATION (HSCT) - REPORT FROM THE XLP REGISTRY
    Bone marrow transplantation
    
    T.G. Gross et al., "CURE OF X-LINKED LYMPHOPROLIFERATIVE DISEASE (XLP) WITH ALLOGENEIC HEMATOPOIETIC STEM-CELL TRANSPLANTATION (HSCT) - REPORT FROM THE XLP REGISTRY", Bone marrow transplantation, 17(5), 1996, pp. 741-744
39. HERROD HG; RABY RB; VALENSKI WR; HUTCHINSON SR; NASTASI KJ; CONLEY ME
    CYTOKINE PRODUCTION AND IGE IN WISKOTT-ALDRICH SYNDROME (WAS) PATIENTS
    Journal of allergy and clinical immunology
    
    H.G. Herrod et al., "CYTOKINE PRODUCTION AND IGE IN WISKOTT-ALDRICH SYNDROME (WAS) PATIENTS", Journal of allergy and clinical immunology, 97(1), 1996, pp. 833-833
40. NASTASI KJ; RABY RB; VALENSKI WR; CONLEY ME; HERROD HG
    ANALYSIS OF IN-VITRO AND SERUM IGM PRODUCTION IN WISKOTT-ALDRICH SYNDROME (WAS) PATIENTS
    Journal of allergy and clinical immunology
    
    K.J. Nastasi et al., "ANALYSIS OF IN-VITRO AND SERUM IGM PRODUCTION IN WISKOTT-ALDRICH SYNDROME (WAS) PATIENTS", Journal of allergy and clinical immunology, 97(1), 1996, pp. 834-834
41. FARRAR JE; ROHRER J; CONLEY ME
    NEUTROPENIA IN X-LINKED AGAMMAGLOBULINEMIA
    Clinical immunology and immunopathology
    
    J.E. Farrar et al., "NEUTROPENIA IN X-LINKED AGAMMAGLOBULINEMIA", Clinical immunology and immunopathology, 81(3), 1996, pp. 271-276
42. NASTASI KJ; RABY RB; VALENSKI WR; HUTCHINSON SR; CONLEY ME; HERROD HG
    CYTOKINE PRODUCTION AND IGE IN WISKOTT-ALDRICH SYNDROME (WAS) PATIENTS
    Pediatric research
    
    K.J. Nastasi et al., "CYTOKINE PRODUCTION AND IGE IN WISKOTT-ALDRICH SYNDROME (WAS) PATIENTS", Pediatric research, 39(4), 1996, pp. 62-62
43. YEL L; MINEGISHI Y; COUSTANSMITH E; BUCKLEY RH; TRUBEL H; PACHMAN LM; KITCHINGMAN GR; CAMPANA D; ROHRER J; CONLEY ME
    MUTATIONS IN THE MU HEAVY-CHAIN GENE IN PATIENTS WITH AGAMMAGLOBULINEMIA
    The New England journal of medicine
    
    L. Yel et al., "MUTATIONS IN THE MU HEAVY-CHAIN GENE IN PATIENTS WITH AGAMMAGLOBULINEMIA", The New England journal of medicine, 335(20), 1996, pp. 1486-1493
44. ROHRER J; RIBEIRO RC; AUERBACH AD; MIRRO B; CONLEY ME
    WISKOTT-ALDRICH SYNDROME IN A FAMILY WITH FANCONI-ANEMIA
    The Journal of pediatrics
    
    J. Rohrer et al., "WISKOTT-ALDRICH SYNDROME IN A FAMILY WITH FANCONI-ANEMIA", The Journal of pediatrics, 129(1), 1996, pp. 50-55
45. SILVENNOINEN O; NISHIGAKI H; KITANAKA A; KUMAGAI MA; ITO C; MALAVASI F; LIN Q; CONLEY ME; CAMPANA D
    CD38 SIGNAL-TRANSDUCTION IN HUMAN B-CELL PRECURSORS - RAPID INDUCTIONOF TYROSINE PHOSPHORYLATION, ACTIVATION OF SYK TYROSINE KINASE, AND PHOSPHORYLATION OF PHOSPHOLIPASE C-GAMMA AND PHOSPHATIDYLINOSITOL 3-KINASE
    The Journal of immunology
    
    O. Silvennoinen et al., "CD38 SIGNAL-TRANSDUCTION IN HUMAN B-CELL PRECURSORS - RAPID INDUCTIONOF TYROSINE PHOSPHORYLATION, ACTIVATION OF SYK TYROSINE KINASE, AND PHOSPHORYLATION OF PHOSPHOLIPASE C-GAMMA AND PHOSPHATIDYLINOSITOL 3-KINASE", The Journal of immunology, 156(1), 1996, pp. 100-107
46. LIN Q; ROHRER J; ALLEN RC; LARCHE M; GREENE JM; SHIGEOKA AO; GATTI RA; DERAUF DC; BELMONT JW; CONLEY ME
    A SINGLE-STRAND CONFORMATION POLYMORPHISM STUDY OF CD40 LIGAND - EFFICIENT MUTATION ANALYSIS AND CARRIER DETECTION FOR X-LINKED HYPER IGM SYNDROME
    The Journal of clinical investigation
    
    Q. Lin et al., "A SINGLE-STRAND CONFORMATION POLYMORPHISM STUDY OF CD40 LIGAND - EFFICIENT MUTATION ANALYSIS AND CARRIER DETECTION FOR X-LINKED HYPER IGM SYNDROME", The Journal of clinical investigation, 97(1), 1996, pp. 196-201
47. CONLEY ME; PAPAROZZI ET; PAIR JC; STROUP WW
    LEAF TATTER IN ACER-SACCHARUM - AN ANATOMICAL LINK
    International journal of plant sciences
    
    M.E. Conley et al., "LEAF TATTER IN ACER-SACCHARUM - AN ANATOMICAL LINK", International journal of plant sciences, 156(3), 1995, pp. 303-310
48. MATHEW P; CONLEY ME
    EFFECT OF INTRAVENOUS GAMMA-GLOBULIN (IVIG) ON THE PLATELET COUNT IN PATIENTS WITH WISKOTT-ALDRICH SYNDROME
    Pediatric allergy and immunology
    
    P. Mathew e M.E. Conley, "EFFECT OF INTRAVENOUS GAMMA-GLOBULIN (IVIG) ON THE PLATELET COUNT IN PATIENTS WITH WISKOTT-ALDRICH SYNDROME", Pediatric allergy and immunology, 6(2), 1995, pp. 91-94
49. CONLEY ME
    PRIMARY IMMUNODEFICIENCIES - A FLURRY OF NEW GENES
    Immunology today
    
    M.E. Conley, "PRIMARY IMMUNODEFICIENCIES - A FLURRY OF NEW GENES", Immunology today, 16(7), 1995, pp. 313-315
50. PAROLINI O; ROHRER J; SHAPIRO LH; CONLEY ME
    B-CELL SPECIFIC DEMETHYLATION OF BTK, THE DEFECTIVE GENE IN X-LINKED AGAMMAGLOBULINEMIA
    Immunogenetics
    
    O. Parolini et al., "B-CELL SPECIFIC DEMETHYLATION OF BTK, THE DEFECTIVE GENE IN X-LINKED AGAMMAGLOBULINEMIA", Immunogenetics, 42(2), 1995, pp. 129-135
51. ROHRER J; PAROLINO O; BELMONT JW; CONLEY ME
    THE GENOMIC STRUCTURE OF HUMAN BTK, THE DEFECTIVE GENE IN X-LINKED AGAMMAGLOBULINEMIA (VOL 40, PG 319, 1994)
    Immunogenetics
    
    J. Rohrer et al., "THE GENOMIC STRUCTURE OF HUMAN BTK, THE DEFECTIVE GENE IN X-LINKED AGAMMAGLOBULINEMIA (VOL 40, PG 319, 1994)", Immunogenetics, 42(1), 1995, pp. 76-76
52. CONLEY ME; ROHRER J
    THE SPECTRUM OF MUTATIONS IN BTK THAT CAUSE X-LINKED AGAMMAGLOBULINEMIA
    Clinical immunology and immunopathology
    
    M.E. Conley e J. Rohrer, "THE SPECTRUM OF MUTATIONS IN BTK THAT CAUSE X-LINKED AGAMMAGLOBULINEMIA", Clinical immunology and immunopathology, 76(3), 1995, pp. 192-197
53. CONLEY ME; FITCHHILGENBERG ME; CLEVELAND JL; PAROLINI O; ROHRER J
    SCREENING OF GENOMIC DNA TO IDENTIFY MUTATIONS IN THE GENE FOR BRUTONS TYROSINE KINASE
    Human molecular genetics
    
    M.E. Conley et al., "SCREENING OF GENOMIC DNA TO IDENTIFY MUTATIONS IN THE GENE FOR BRUTONS TYROSINE KINASE", Human molecular genetics, 3(10), 1994, pp. 1751-1756
54. WANG WC; CORDOBA J; INFANTE AJ; CONLEY ME
    SUCCESSFUL TREATMENT OF NEUTROPENIA IN THE HYPER-IMMUNOGLOBULIN-M SYNDROME WITH GRANULOCYTE-COLONY-STIMULATING FACTOR
    The American journal of pediatric hematology/oncology
    
    W.C. Wang et al., "SUCCESSFUL TREATMENT OF NEUTROPENIA IN THE HYPER-IMMUNOGLOBULIN-M SYNDROME WITH GRANULOCYTE-COLONY-STIMULATING FACTOR", The American journal of pediatric hematology/oncology, 16(2), 1994, pp. 160-163
55. CONLEY ME; PAROLINI O; ROHRER J; CAMPANA D
    X-LINKED AGAMMAGLOBULINEMIA - NEW APPROACHES TO OLD QUESTIONS BASED ON THE IDENTIFICATION OF THE DEFECTIVE GENE
    Immunological reviews
    
    M.E. Conley et al., "X-LINKED AGAMMAGLOBULINEMIA - NEW APPROACHES TO OLD QUESTIONS BASED ON THE IDENTIFICATION OF THE DEFECTIVE GENE", Immunological reviews, 138, 1994, pp. 5-21
56. ROHRER J; PAROLINO O; BELMONT JW; CONLEY ME
    THE GENOMIC STRUCTURE OF HUMAN BTK, THE DEFECTIVE GENE IN X-LINKED AGAMMAGLOBULINEMIA
    Immunogenetics
    
    J. Rohrer et al., "THE GENOMIC STRUCTURE OF HUMAN BTK, THE DEFECTIVE GENE IN X-LINKED AGAMMAGLOBULINEMIA", Immunogenetics, 40(5), 1994, pp. 319-324
57. CONLEY ME; ROHRER J; FITCHHILGENBERG MF; PAROLINI O
    VARIABLE CLINICAL CONSEQUENCES OF PREMATURE STOP CODONS IN BTK, THE DEFECTIVE GENE IN X-LINKED AGAMMAGLOBULINEMIA (XLA)
    Pediatric research
    
    M.E. Conley et al., "VARIABLE CLINICAL CONSEQUENCES OF PREMATURE STOP CODONS IN BTK, THE DEFECTIVE GENE IN X-LINKED AGAMMAGLOBULINEMIA (XLA)", Pediatric research, 35(4), 1994, pp. 10000010-10000010
58. PAROLINI O; ROHRER J; CONLEY ME
    ATYPICAL X-LINKED AGAMMAGLOBULINEMIA - REPLY
    The New England journal of medicine
    
    O. Parolini et al., "ATYPICAL X-LINKED AGAMMAGLOBULINEMIA - REPLY", The New England journal of medicine, 331(14), 1994, pp. 950-950
59. SAFFRAN DC; PAROLINI O; FITCHHILGENBERG ME; RAWLINGS DJ; AFAR DEH; WITTE ON; CONLEY ME
    A POINT MUTATION IN THE SH2 DOMAIN OF BRUTONS TYROSINE KINASE IN ATYPICAL X-LINKED AGAMMAGLOBULINEMIA - BRIEF REPORT
    The New England journal of medicine
    
    D.C. Saffran et al., "A POINT MUTATION IN THE SH2 DOMAIN OF BRUTONS TYROSINE KINASE IN ATYPICAL X-LINKED AGAMMAGLOBULINEMIA - BRIEF REPORT", The New England journal of medicine, 330(21), 1994, pp. 1488-1491
60. CONLEY ME; LARCHE M; BONAGURA VR; LAWTON AR; BUCKLEY RH; FU SM; COUSTANSMITH E; HERROD HG; CAMPANA D
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