-
1
-
-
0025253068
-
Glanzmann's thrombasthenia: The spectrum of clinical disease
-
George J N, Caen J P, Nurden A T. Glanzmann's thrombasthenia: The spectrum of clinical disease. Blood. 75:1990;1383-1395.
-
(1990)
Blood
, vol.75
, pp. 1383-1395
-
-
George, J.N.1
Caen, J.P.2
Nurden, A.T.3
-
2
-
-
0028028267
-
Glanzmann thrombasthenia: New insights from an historical perspective
-
Coller B S, Seligsohn U, Peretz H, Newman P J. Glanzmann thrombasthenia: New insights from an historical perspective. Semin Hematol. 31:1994;301-311.
-
(1994)
Semin Hematol
, vol.31
, pp. 301-311
-
-
Coller, B.S.1
Seligsohn, U.2
Peretz, H.3
Newman, P.J.4
-
3
-
-
0023664558
-
Structure of the platelet membrane glycoprotein IIb
-
Poncz M, Eisman R, Heidenreich R. Structure of the platelet membrane glycoprotein IIb. J Biol Chem. 262:1987;8476-8482.
-
(1987)
J Biol Chem
, vol.262
, pp. 8476-8482
-
-
Poncz, M.1
Eisman, R.2
Heidenreich, R.3
-
4
-
-
0023189463
-
Protein sequence of endothelial glycoprotein IIIa derived from a cDNA clone
-
Fitzgerald L A, Steiner B, Rall S C Jr., Lo S, Phillips D R. Protein sequence of endothelial glycoprotein IIIa derived from a cDNA clone. J Biol Chem. 262:1987;3936-3939.
-
(1987)
J Biol Chem
, vol.262
, pp. 3936-3939
-
-
Fitzgerald, L.A.1
Steiner, B.2
Rall S.C., Jr.3
Lo, S.4
Phillips, D.R.5
-
6
-
-
0029797046
-
Mutation nomenclature: Nicknames, systematic names, and unique identifiers
-
Beutler E, McKusick V A, Motulsky A G, Scriver C R, Hutchinson F. Mutation nomenclature: Nicknames, systematic names, and unique identifiers. Hum Mutat. 8:1996;203-206.
-
(1996)
Hum Mutat
, vol.8
, pp. 203-206
-
-
Beutler, E.1
McKusick, V.A.2
Motulsky, A.G.3
Scriver, C.R.4
Hutchinson, F.5
-
7
-
-
0026035227
-
A deletion in the gene for glycoprotein IIb associated with Glanzmann's thrombasthenia
-
Burk C D, Newman P J, Lyman S, Gill J, Coller B S, Poncz M. A deletion in the gene for glycoprotein IIb associated with Glanzmann's thrombasthenia. J Clin Invest. 87:1991;270-276.
-
(1991)
J Clin Invest
, vol.87
, pp. 270-276
-
-
Burk, C.D.1
Newman, P.J.2
Lyman, S.3
Gill, J.4
Coller, B.S.5
Poncz, M.6
-
8
-
-
0022597477
-
Immunologic and biochemical characterization of homozygous and heterozygous Glanzmann thrombasthenia in the Iraqi-Jewish and Arab populations in Israel: Comparison of techniques for carrier detection
-
Coller B S, Seligsohn U, Zivelin A, Zwang E, Lusky A, Modan M. Immunologic and biochemical characterization of homozygous and heterozygous Glanzmann thrombasthenia in the Iraqi-Jewish and Arab populations in Israel: comparison of techniques for carrier detection. Br J Haematol. 62:1986;723-735.
-
(1986)
Br J Haematol
, vol.62
, pp. 723-735
-
-
Coller, B.S.1
Seligsohn, U.2
Zivelin, A.3
Zwang, E.4
Lusky, A.5
Modan, M.6
-
9
-
-
0023234277
-
Type I Glanzmann thrombasthenia patients from the Iraqi-Jewish and Arab populations in Israel can be differentiated by platelet glycoprotein IIIa immunoblot analysis
-
Coller B S, Seligsohn S, Little P A. Type I Glanzmann thrombasthenia patients from the Iraqi-Jewish and Arab populations in Israel can be differentiated by platelet glycoprotein IIIa immunoblot analysis. Blood. 69:1987;1969-1703.
-
(1987)
Blood
, vol.69
, pp. 1969-1703
-
-
Coller, B.S.1
Seligsohn, S.2
Little, P.A.3
-
10
-
-
0024410402
-
Immunoblot analysis of platelet glycoprotein IIb in patients with Glanzmann thrombasthenia in Israel
-
Seligsohn U, Coller B S, Zivelin A, Plow E F, Ginsberg M H. Immunoblot analysis of platelet glycoprotein IIb in patients with Glanzmann thrombasthenia in Israel. Br J Haematol. 72:1989;415-423.
-
(1989)
Br J Haematol
, vol.72
, pp. 415-423
-
-
Seligsohn, U.1
Coller, B.S.2
Zivelin, A.3
Plow, E.F.4
Ginsberg, M.H.5
-
11
-
-
0026024976
-
Platelet vitronectin receptor expression differentiates Iraqi-Jewish from Arab patients with Glanzmann thrombasthenia in Israel
-
Coller B S, Cheresh D A, Asch E, Seligsohn U. Platelet vitronectin receptor expression differentiates Iraqi-Jewish from Arab patients with Glanzmann thrombasthenia in Israel. Blood. 77:1991;75-83.
-
(1991)
Blood
, vol.77
, pp. 75-83
-
-
Coller, B.S.1
Cheresh, D.A.2
Asch, E.3
Seligsohn, U.4
-
12
-
-
0026356066
-
The molecular genetic basis of Glanzmann thrombasthenia in the Iraqi-Jewish and Arab populations in Israel
-
Newman P J, Seligsohn U, Lyman S, Coller B S. The molecular genetic basis of Glanzmann thrombasthenia in the Iraqi-Jewish and Arab populations in Israel. Proc Natl Acad Sci USA. 88:1991;3160-3164.
-
(1991)
Proc Natl Acad Sci USA
, vol.88
, pp. 3160-3164
-
-
Newman, P.J.1
Seligsohn, U.2
Lyman, S.3
Coller, B.S.4
-
13
-
-
0343033819
-
A new variant of Glanzmann thrombasthenia (Frankfurt I)
-
Kirchmaier C M, Westrup D, Becker-Hagendorff K, Just M, Jablonka B, Seifried E. A new variant of Glanzmann thrombasthenia (Frankfurt I). Thromb Haemost. 73:1995;1058.
-
(1995)
Thromb Haemost
, vol.73
, pp. 1058
-
-
Kirchmaier, C.M.1
Westrup, D.2
Becker-Hagendorff, K.3
Just, M.4
Jablonka, B.5
Seifried, E.6
-
14
-
-
0342599549
-
Glanzmann thrombasthenia due to a glycoprotein IIb missense mutation Leu214Pro
-
Chen F P, Coller B S, Weiss H J, Xu L Z, French D L. Glanzmann thrombasthenia due to a glycoprotein IIb missense mutation Leu214Pro. Thromb Haemost. 73:1995;1191.
-
(1995)
Thromb Haemost
, vol.73
, pp. 1191
-
-
Chen, F.P.1
Coller, B.S.2
Weiss, H.J.3
Xu, L.Z.4
French, D.L.5
-
15
-
-
0343033817
-
-
C, M, Grimaldi, F, P, Chen, C, H, Wu, H, J, Weiss, B, S, Coller, D, L, French, 1997, Glanzmann thrombasthenia due to a glycoprotein IIb missense mutation Leu214Pro identifies a region important in ligand binding.
-
(1997)
Glanzmann Thrombasthenia Due to a Glycoprotein IIb Missense Mutation Leu214Pro Identifies a Region Important in Ligand Binding
-
-
Grimaldi, C.M.1
Chen, F.P.2
Wu, C.H.3
Weiss, H.J.4
Coller, B.S.5
French, D.L.6
-
16
-
-
0028123329
-
Glanzmann thrombasthenia secondary to a Gly273Asp mutation adjacent to the first calcium-binding domain of platelet glycoprotein IIb
-
Poncz M, Rifat S, Coller B S, Newman P J, Shattil S J, Parrella T, Fortina P, Bennett J S. Glanzmann thrombasthenia secondary to a Gly273Asp mutation adjacent to the first calcium-binding domain of platelet glycoprotein IIb. J Clin Invest. 93:1994;172-179.
-
(1994)
J Clin Invest
, vol.93
, pp. 172-179
-
-
Poncz, M.1
Rifat, S.2
Coller, B.S.3
Newman, P.J.4
Shattil, S.J.5
Parrella, T.6
Fortina, P.7
Bennett, J.S.8
-
18
-
-
0028951764
-
Glanzmann thrombasthenia resulting from a single amino acid substitution between the second and third calcium-binding domains of GPIIb
-
Wilcox D A, Paddock C M, Lyman S, Gill J C, Newman P J. Glanzmann thrombasthenia resulting from a single amino acid substitution between the second and third calcium-binding domains of GPIIb. J Clin Invest. 95:1995;1553-1560.
-
(1995)
J Clin Invest
, vol.95
, pp. 1553-1560
-
-
Wilcox, D.A.1
Paddock, C.M.2
Lyman, S.3
Gill, J.C.4
Newman, P.J.5
-
19
-
-
0029658260
-
A mutant (Arg327→His) GPIIb associated to thrombathenia exerts a dominant negative effect in stably transfected CHO cells
-
Ferrer M, Fernandez-Pinel M, Gonzalez-Manchon C, Gonzalez J, Ayuso M S, Parrilla R. A mutant (Arg327→His) GPIIb associated to thrombathenia exerts a dominant negative effect in stably transfected CHO cells. Thromb and Haemost. 76:1996;292-301.
-
(1996)
Thromb and Haemost
, vol.76
, pp. 292-301
-
-
Ferrer, M.1
Fernandez-Pinel, M.2
Gonzalez-Manchon, C.3
Gonzalez, J.4
Ayuso, M.S.5
Parrilla, R.6
-
23
-
-
4243631519
-
A common Arg584Stop mutation in glycoprotein (GP) IIb in 2 additional patients with Glanzmann thrombasthenia
-
French D L, Chen F P, Xu L, Coller B S. A common Arg584Stop mutation in glycoprotein (GP) IIb in 2 additional patients with Glanzmann thrombasthenia. Blood. 88:1996;30a.
-
(1996)
Blood
, vol.88
-
-
French, D.L.1
Chen, F.P.2
Xu, L.3
Coller, B.S.4
-
24
-
-
0025731751
-
Analysis of a variant form of platelet glycoprotein (GP) IIb: A second patient with abnormal molecular weight GPIIb
-
Moroi M, Yamamura J, Koga H, Miyazaki S, Jung S M. Analysis of a variant form of platelet glycoprotein (GP) IIb: a second patient with abnormal molecular weight GPIIb. Thromb Res. 62:1991;217-225.
-
(1991)
Thromb Res
, vol.62
, pp. 217-225
-
-
Moroi, M.1
Yamamura, J.2
Koga, H.3
Miyazaki, S.4
Jung, S.M.5
-
25
-
-
0026711020
-
Molecular basis for Glanzmann's thrombasthenia (GT) in a compound heterozygote with glycoprotein IIb gene: A proposal for the classification of GT based on the biosynthetic pathway of glycoprotein IIb-IIIa complex
-
Kato A, Yamamoto K, Miyazaki S, Jung S M, Moroi M, Aoki N. Molecular basis for Glanzmann's thrombasthenia (GT) in a compound heterozygote with glycoprotein IIb gene: A proposal for the classification of GT based on the biosynthetic pathway of glycoprotein IIb-IIIa complex. Blood. 79:1992;3212-3218.
-
(1992)
Blood
, vol.79
, pp. 3212-3218
-
-
Kato, A.1
Yamamoto, K.2
Miyazaki, S.3
Jung, S.M.4
Moroi, M.5
Aoki, N.6
-
26
-
-
0027473163
-
Application of GPIIIa gene Taq I polymorphism to determination of carrier status in Glanzmann's thrombasthenia families of Chinese origin
-
Ruan C G, Gu J M, Wang X D, Chu X H, Pan J L. Application of GPIIIa gene Taq I polymorphism to determination of carrier status in Glanzmann's thrombasthenia families of Chinese origin. Thromb Haemost. 68:1993;64-69.
-
(1993)
Thromb Haemost
, vol.68
, pp. 64-69
-
-
Ruan, C.G.1
Gu, J.M.2
Wang, X.D.3
Chu, X.H.4
Pan, J.L.5
-
27
-
-
0027447751
-
Identification of a nonsense mutation at amino acid 584-arginine of platelet glycoprotein IIb in patients with type I Glanzmann thrombasthenia
-
Gu J M, Xu W F, Wang X D, Wu Q Y, Chi C W, Ruan C G. Identification of a nonsense mutation at amino acid 584-arginine of platelet glycoprotein IIb in patients with type I Glanzmann thrombasthenia. Br J Haematol. 83:1993;442-449.
-
(1993)
Br J Haematol
, vol.83
, pp. 442-449
-
-
Gu, J.M.1
Xu, W.F.2
Wang, X.D.3
Wu, Q.Y.4
Chi, C.W.5
Ruan, C.G.6
-
28
-
-
0029153950
-
Molecular study of Glanzmann thrombasthenia in 3 patients issued from 2 different families
-
Vinciguerra C, Trzeciak M C, Philippe N. Molecular study of Glanzmann thrombasthenia in 3 patients issued from 2 different families. Thromb Haemost. 74:1994;822-827.
-
(1994)
Thromb Haemost
, vol.74
, pp. 822-827
-
-
Vinciguerra, C.1
Trzeciak, M.C.2
Philippe, N.3
-
29
-
-
0028342658
-
Demonstration of a marked reduction in the amount of GPIIb in most type II patients with Glanzmann's thrombasthenia
-
Tomiyama Y, Kashiwagi H, Kosugi S. Demonstration of a marked reduction in the amount of GPIIb in most type II patients with Glanzmann's thrombasthenia. Br J Haematol. 87:1994;119-124.
-
(1994)
Br J Haematol
, vol.87
, pp. 119-124
-
-
Tomiyama, Y.1
Kashiwagi, H.2
Kosugi, S.3
-
30
-
-
0029071549
-
Abnormal processing of the glycoprotein IIb transcript due to a nonsense mutation in exon 17 associated with Glanzmann's thrombasthenia
-
Tomiyama Y, Kashiwagi H, Kosugi S. Abnormal processing of the glycoprotein IIb transcript due to a nonsense mutation in exon 17 associated with Glanzmann's thrombasthenia. Thromb Haemost. 73:1995;756-762.
-
(1995)
Thromb Haemost
, vol.73
, pp. 756-762
-
-
Tomiyama, Y.1
Kashiwagi, H.2
Kosugi, S.3
-
31
-
-
0028936301
-
Glanzmann's thrombasthenia associated with deletion-insertion and alternative splicing in the glycoprotein IIb gene
-
Peretz H, Rosenberg N, Usher S. Glanzmann's thrombasthenia associated with deletion-insertion and alternative splicing in the glycoprotein IIb gene. Blood. 85:1995;414-420.
-
(1995)
Blood
, vol.85
, pp. 414-420
-
-
Peretz, H.1
Rosenberg, N.2
Usher, S.3
-
32
-
-
0028117258
-
An exon 28 mutation resulting in alternative splicing of the glycoprotein IIb transcript and Glanzmann's thrombasthenia
-
Iwamoto S, Nishiumi E, Kajii E, Ikemoto S. An exon 28 mutation resulting in alternative splicing of the glycoprotein IIb transcript and Glanzmann's thrombasthenia. Blood. 83:1994;1017-1023.
-
(1994)
Blood
, vol.83
, pp. 1017-1023
-
-
Iwamoto, S.1
Nishiumi, E.2
Kajii, E.3
Ikemoto, S.4
-
33
-
-
0025996473
-
Effect of deletion of glycoprotein Iib exon 28 on the expression of the platelet glycoprotein Iib/IIIa complex
-
Kolodziej M A, Vilaire D, Rifat S, Poncz M, Bennett J S. Effect of deletion of glycoprotein Iib exon 28 on the expression of the platelet glycoprotein Iib/IIIa complex. Blood. 78:1991;22344-22353.
-
(1991)
Blood
, vol.78
, pp. 22344-22353
-
-
Kolodziej, M.A.1
Vilaire, D.2
Rifat, S.3
Poncz, M.4
Bennett, J.S.5
-
34
-
-
0022646192
-
Platelet adhesion and thrombus formation on subendothelium in platelets deficient in glycoproteins IIb-IIIa, Ib, and storage granules
-
Weiss H J, Turitto V T, Baumgartner H R. Platelet adhesion and thrombus formation on subendothelium in platelets deficient in glycoproteins IIb-IIIa, Ib, and storage granules. Blood. 67:1986;322-330.
-
(1986)
Blood
, vol.67
, pp. 322-330
-
-
Weiss, H.J.1
Turitto, V.T.2
Baumgartner, H.R.3
-
35
-
-
0343905343
-
Two unrelated doubly heterozygous patients with Glanzmann thrombasthenia have the same GPIIb mutation resulting in loss of the transmembrane domain
-
Florence, Italy
-
D, L, French, F, P, Chen, L, Xu, H, J, Weiss, B, S, Coller, 1997, Two unrelated doubly heterozygous patients with Glanzmann thrombasthenia have the same GPIIb mutation resulting in loss of the transmembrane domain, XVIth Congress of the ISTH, Florence, Italy.
-
(1997)
XVIth Congress of the ISTH
-
-
French, D.L.1
Chen, F.P.2
Xu, L.3
Weiss, H.J.4
Coller, B.S.5
-
36
-
-
0014241907
-
Studies of platelet function and proteins in three patients with Glanzmann thrombasthenia
-
Weiss H J, Kockwa S. Studies of platelet function and proteins in three patients with Glanzmann thrombasthenia. J Lab Clin Med. 71:1968;153-165.
-
(1968)
J Lab Clin Med
, vol.71
, pp. 153-165
-
-
Weiss, H.J.1
Kockwa, S.2
-
37
-
-
0026772036
-
A defect of platelet aggregation with an abnormal distribution of glycoprotein IIb-IIIa complexes within the platelet
-
Hardisty R, Pidard D, Cox A. A defect of platelet aggregation with an abnormal distribution of glycoprotein IIb-IIIa complexes within the platelet. Blood. 80:1992;696-708.
-
(1992)
Blood
, vol.80
, pp. 696-708
-
-
Hardisty, R.1
Pidard, D.2
Cox, A.3
-
39
-
-
0027499394
-
Glanzmann's thrombasthenia caused by homozygosity for a splice defect that leads to deletion of the first coding exon of the glycoprotein IIIa mRNA
-
Simsek S, Heyboer H, de Bruijne-Admiraal L G, Goldschmeding R, Cuijpers H TM, von dem Borne A EGK. Glanzmann's thrombasthenia caused by homozygosity for a splice defect that leads to deletion of the first coding exon of the glycoprotein IIIa mRNA. Blood. 81:1993;2044-2049.
-
(1993)
Blood
, vol.81
, pp. 2044-2049
-
-
Simsek, S.1
Heyboer, H.2
De Bruijne-Admiraal, L.G.3
Goldschmeding, R.4
Cuijpers, H.T.M.5
Von Dem Borne A. Egk6
-
41
-
-
0022982040
-
Divalent cation regulation of the surface orientation of platelet membrane glycoprotein IIb. Correlation with fibrinogen binding function and definition of a novel variant of Glanzmann's thrombasthenia
-
Ginsberg M H, Lightsey A, Kunicki T J, Kaufmann A, Marguerie G, Plow E F. Divalent cation regulation of the surface orientation of platelet membrane glycoprotein IIb. Correlation with fibrinogen binding function and definition of a novel variant of Glanzmann's thrombasthenia. J Clin Invest. 78:1986;1103-1111.
-
(1986)
J Clin Invest
, vol.78
, pp. 1103-1111
-
-
Ginsberg, M.H.1
Lightsey, A.2
Kunicki, T.J.3
Kaufmann, A.4
Marguerie, G.5
Plow, E.F.6
-
43
-
-
85030293922
-
-
C, Ward, Y, L, Chao, P, Bray, P, J, Newman, 1997
-
C, Ward, Y, L, Chao, P, Bray, P, J, Newman, 1997.
-
-
-
-
47
-
-
0028070770
-
Activation of the fibrinogen binding site on platelets isolated from a patient with the Strasbourg I variant of Glanzmann's thrombasthenia
-
Kouns W C, Steiner B, Kunicki T J. Activation of the fibrinogen binding site on platelets isolated from a patient with the Strasbourg I variant of Glanzmann's thrombasthenia. Blood. 84:1994;1108-1115.
-
(1994)
Blood
, vol.84
, pp. 1108-1115
-
-
Kouns, W.C.1
Steiner, B.2
Kunicki, T.J.3
-
48
-
-
0023104863
-
A variant of Glanzmann's thrombasthenia with abnormal glycoprotein IIb-IIIa complexes in the platelet membrane
-
Nurden A T, Rosa J-P, Fournier D. A variant of Glanzmann's thrombasthenia with abnormal glycoprotein IIb-IIIa complexes in the platelet membrane. J Clin Invest. 79:1987;962-969.
-
(1987)
J Clin Invest
, vol.79
, pp. 962-969
-
-
Nurden, A.T.1
Rosa J-P2
Fournier, D.3
-
50
-
-
0024367855
-
A variant of Glanzmann's thrombasthenia characterized by abnormal glycoprotein IIb/IIIa complex formation
-
Fournier D J, Kabral A, Castaldi P A, Berndt M C. A variant of Glanzmann's thrombasthenia characterized by abnormal glycoprotein IIb/IIIa complex formation. Thromb Haemost. 62:1989;977-983.
-
(1989)
Thromb Haemost
, vol.62
, pp. 977-983
-
-
Fournier, D.J.1
Kabral, A.2
Castaldi, P.A.3
Berndt, M.C.4
-
52
-
-
0000650163
-
Type II Glanzmann thrombasthenia due to a destabilizing amino acid substitution in platelet membrane glycoprotein IIIa
-
Newman P J, Weyerbusch-Bottum S, Visentin G P, Gidwitz S, White G C II. Type II Glanzmann thrombasthenia due to a destabilizing amino acid substitution in platelet membrane glycoprotein IIIa. Thromb Haemost. 69:1993;1017.
-
(1993)
Thromb Haemost
, vol.69
, pp. 1017
-
-
Newman, P.J.1
Weyerbusch-Bottum, S.2
Visentin, G.P.3
Gidwitz, S.4
White G.C. II5
-
53
-
-
0025178671
-
Identification of an abnormal gene for the GPIIIa subunit of the platelet fibrinogen receptor resulting in Glanzmann thrombasthenia
-
Bray P F, Shuman M A. Identification of an abnormal gene for the GPIIIa subunit of the platelet fibrinogen receptor resulting in Glanzmann thrombasthenia. Blood. 75:1990;881-888.
-
(1990)
Blood
, vol.75
, pp. 881-888
-
-
Bray, P.F.1
Shuman, M.A.2
-
54
-
-
0027437275
-
Homologous recombination among three intragene Alu sequences causes an inversion-deletion resulting in the hereditary bleeding disorder Glanzmann thrombasthenia
-
Li L, Bray P G. Homologous recombination among three intragene Alu sequences causes an inversion-deletion resulting in the hereditary bleeding disorder Glanzmann thrombasthenia. Am J Hum Genet. 53:1993;140-149.
-
(1993)
Am J Hum Genet
, vol.53
, pp. 140-149
-
-
Li, L.1
Bray, P.G.2
-
55
-
-
0027367949
-
Single-strand conformation polymorphism analysis is a rapid and effective method for the identification of mutations and polymorphisms in the gene for glycoprotein IIIa
-
Jin Y, Dietz H C, Nurden A, Bray P F. Single-strand conformation polymorphism analysis is a rapid and effective method for the identification of mutations and polymorphisms in the gene for glycoprotein IIIa. Blood. 82:1993;2281-2288.
-
(1993)
Blood
, vol.82
, pp. 2281-2288
-
-
Jin, Y.1
Dietz, H.C.2
Nurden, A.3
Bray, P.F.4
-
56
-
-
85030292409
-
-
C, Ward, A, Kestin, P, J, Newman, 1997
-
C, Ward, A, Kestin, P, J, Newman, 1997.
-
-
-
-
58
-
-
85058206635
-
The GPIIIa Cys374-Cys386 disulfide loop is important for biosynthesis and function of the GPIIb/IIIa receptor
-
Grimaldi C M, Coller B S, French D L. The GPIIIa Cys374-Cys386 disulfide loop is important for biosynthesis and function of the GPIIb/IIIa receptor. Blood. 88:1996;279a.
-
(1996)
Blood
, vol.88
-
-
Grimaldi, C.M.1
Coller, B.S.2
French, D.L.3
-
60
-
-
0029910219
-
Glanzmann thrombasthenia. Cooperation between sequence variants incis
-
Jin Y, Dietz H C, Montgomery R A. Glanzmann thrombasthenia. Cooperation between sequence variants incis. J Clin Invest. 98:1996;1745-1754.
-
(1996)
J Clin Invest
, vol.98
, pp. 1745-1754
-
-
Jin, Y.1
Dietz, H.C.2
Montgomery, R.A.3
|