Bernard-Soulier syndrome associated with 22q11.2 microdeletion.
about
CHD associated with syndromic diagnoses: peri-operative risk factors and early outcomes.The molecular basis of congenital thrombocytopenias: insights into megakaryopoiesis.Hematological abnormalities and 22q11.2 deletion syndrome.A review of inherited platelet disorders with guidelines for their management on behalf of the UKHCDO.Deletion 16p13.11 uncovers NDE1 mutations on the non-deleted homolog and extends the spectrum of severe microcephaly to include fetal brain disruption.
P2860
Bernard-Soulier syndrome associated with 22q11.2 microdeletion.
description
2001 nî lūn-bûn
@nan
2001 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年学术文章
@wuu
2001年学术文章
@zh-cn
2001年学术文章
@zh-hans
2001年学术文章
@zh-my
2001年学术文章
@zh-sg
2001年學術文章
@yue
name
Bernard-Soulier syndrome associated with 22q11.2 microdeletion.
@ast
Bernard-Soulier syndrome associated with 22q11.2 microdeletion.
@en
Bernard-Soulier syndrome associated with 22q11.2 microdeletion.
@nl
type
label
Bernard-Soulier syndrome associated with 22q11.2 microdeletion.
@ast
Bernard-Soulier syndrome associated with 22q11.2 microdeletion.
@en
Bernard-Soulier syndrome associated with 22q11.2 microdeletion.
@nl
prefLabel
Bernard-Soulier syndrome associated with 22q11.2 microdeletion.
@ast
Bernard-Soulier syndrome associated with 22q11.2 microdeletion.
@en
Bernard-Soulier syndrome associated with 22q11.2 microdeletion.
@nl
P2093
P2860
P1476
Bernard-Soulier syndrome associated with 22q11.2 microdeletion.
@en
P2093
P2860
P304
P356
10.1002/1096-8628(2001)9999:9999<::AID-AJMG1176>3.0.CO;2-T
P577
2001-04-01T00:00:00Z