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Results: 1-7 |
Results: 7
GLANZMANN THROMBASTHENIA IN 2 IRAQI-JEWISH SIBLINGS IS CAUSED BY A NOVEL SPLICE JUNCTION MUTATION IN THE GLYCOPROTEIN IIB
Authors: YATUV R ROSENBERG N DARDIK R BRENNER B SELIGSOHN U
Citation: R. Yatuv et al., GLANZMANN THROMBASTHENIA IN 2 IRAQI-JEWISH SIBLINGS IS CAUSED BY A NOVEL SPLICE JUNCTION MUTATION IN THE GLYCOPROTEIN IIB, Blood coagulation & fibrinolysis, 9(3), 1998, pp. 285-288
GLYCOPROTEIN IIIA TRUNCATION RATHER THAN ABSENCE OF CYSTEINE(406)-CYSTEINE(665) BOND CAUSES THROMBASTHENIA IN MOST IRAQI-JEWISH PATIENTS
Authors: YATUV R ROSENBERG N DARDIK R SELIGSOHN U
Citation: R. Yatuv et al., GLYCOPROTEIN IIIA TRUNCATION RATHER THAN ABSENCE OF CYSTEINE(406)-CYSTEINE(665) BOND CAUSES THROMBASTHENIA IN MOST IRAQI-JEWISH PATIENTS, British Journal of Haematology, 102(1), 1998, pp. 285-285
A 3RD MUTATION CAUSING THROMBASTHENIA IN IRAQI-JEWS
Authors: YATUV R ROSENBERG N DARDIK R BRENNER B SELIGSOHN U
Citation: R. Yatuv et al., A 3RD MUTATION CAUSING THROMBASTHENIA IN IRAQI-JEWS, Thrombosis and haemostasis, 1997, pp. 1477-1477
GLANZMANN THROMBASTHENIA CAUSED BY AN 11.2-KB DELETION IN THE GLYCOPROTEIN IIIA (BETA(3)) IS A 2ND MUTATION IN IRAQI JEWS THAT STEMMED FROMA DISTINCT FOUNDER
Authors: ROSENBERG N YATUV R ORION Y ZIVELIN A DARDIK R PERETZ H SELIGSOHN U
Citation: N. Rosenberg et al., GLANZMANN THROMBASTHENIA CAUSED BY AN 11.2-KB DELETION IN THE GLYCOPROTEIN IIIA (BETA(3)) IS A 2ND MUTATION IN IRAQI JEWS THAT STEMMED FROMA DISTINCT FOUNDER, Blood, 89(10), 1997, pp. 3654-3662
THE 11BP DELETION IN GLYCOPROTEIN IIIA WHICH CAUSES GLANZMANN THROMBASTHENIA IN IRAQI-JEWS PROBABLY STEMS FROM A COMMON FOUNDER
Authors: ROSENBERG N YATUV R PERETZ H SELIGSOHN U
Citation: N. Rosenberg et al., THE 11BP DELETION IN GLYCOPROTEIN IIIA WHICH CAUSES GLANZMANN THROMBASTHENIA IN IRAQI-JEWS PROBABLY STEMS FROM A COMMON FOUNDER, Thrombosis and haemostasis, 73(6), 1995, pp. 1189-1189
COMBINED FACTOR-V AND FACTOR-VIII DEFICIENCY IS PROBABLY NOT RELATED TO GENETIC-DISORDERS OF COMPONENTS OF THE PROTEIN-C SYSTEM
Authors: ZIVELIN A YATUV R SELIGSOHN U
Citation: A. Zivelin et al., COMBINED FACTOR-V AND FACTOR-VIII DEFICIENCY IS PROBABLY NOT RELATED TO GENETIC-DISORDERS OF COMPONENTS OF THE PROTEIN-C SYSTEM, Thrombosis and haemostasis, 73(6), 1995, pp. 1439-1439
ONE OF THE 2 COMMON MUTATIONS CAUSING FACTOR-XI DEFICIENCY IN ASHKENAZI JEWS (TYPE-II) IS ALSO PREVALENT IN IRAQI JEWS, WHO REPRESENT THE ANCIENT GENE POOL OF JEWS
Authors: SHPILBERG O PERETZ H ZIVELIN A YATUV R CHETRIT A KULKA T STERN C WEISS E SELIGSOHN U
Citation: O. Shpilberg et al., ONE OF THE 2 COMMON MUTATIONS CAUSING FACTOR-XI DEFICIENCY IN ASHKENAZI JEWS (TYPE-II) IS ALSO PREVALENT IN IRAQI JEWS, WHO REPRESENT THE ANCIENT GENE POOL OF JEWS, Blood, 85(2), 1995, pp. 429-432
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