Prenatal diagnosis of Glanzmann thrombasthenia using the polymorphic markers BRCA1 and THRA1 on chromosome 17.
about
Glanzmann thrombastheniaThe GPIIb/IIIa (integrin alphaIIbbeta3) odyssey: a technology-driven saga of a receptor with twists, turns, and even a bend.The platelet: life on the razor's edge between hemorrhage and thrombosis.Historical perspective and future directions in platelet research.Founder effect and estimation of the age of the French Gypsy mutation associated with Glanzmann thrombasthenia in Manouche familiesTranslating from the rivers of Babylon to the coronary bloodstreamWheat-related disorders: A broad spectrum of 'evolving' diseasesA 13-bp deletion in alpha(IIb) gene is a founder mutation that predominates in Palestinian-Arab patients with Glanzmann thrombasthenia.Clinical utility gene card for: Glanzmann thrombasthenia.Intrauterine red cell transfusion for anti-Kell isoimmunization in a fetus with Glanzmann's thrombasthenia.
P2860
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P2860
Prenatal diagnosis of Glanzmann thrombasthenia using the polymorphic markers BRCA1 and THRA1 on chromosome 17.
description
1998 nî lūn-bûn
@nan
1998年の論文
@ja
1998年学术文章
@wuu
1998年学术文章
@zh-cn
1998年学术文章
@zh-hans
1998年学术文章
@zh-my
1998年学术文章
@zh-sg
1998年學術文章
@yue
1998年學術文章
@zh
1998年學術文章
@zh-hant
name
Prenatal diagnosis of Glanzman ...... A1 and THRA1 on chromosome 17.
@en
Prenatal diagnosis of Glanzman ...... A1 and THRA1 on chromosome 17.
@nl
type
label
Prenatal diagnosis of Glanzman ...... A1 and THRA1 on chromosome 17.
@en
Prenatal diagnosis of Glanzman ...... A1 and THRA1 on chromosome 17.
@nl
prefLabel
Prenatal diagnosis of Glanzman ...... A1 and THRA1 on chromosome 17.
@en
Prenatal diagnosis of Glanzman ...... A1 and THRA1 on chromosome 17.
@nl
P2093
P2860
P1476
Prenatal diagnosis of Glanzman ...... A1 and THRA1 on chromosome 17.
@en
P2093
Berkowitz R
Seligsohn U
P2860
P304
P356
10.1046/J.1365-2141.1998.00798.X
P407
P577
1998-07-01T00:00:00Z