Severe haemophilia A in a female: a compound heterozygote with nonrandom X-inactivation.
about
Mutation spectrum of 122 hemophilia A families from Taiwanese population by LD-PCR, DHPLC, multiplex PCR and evaluating the clinical application of HRMHaemophilia A: molecular insights.A hemophilic son of a hemophiliac: did my son inherit my hemophilia?Investigation of inflicted injury in a young girl reveals mild haemophilia A and Turner's syndrome.Identification of 123 previously unreported mutations in the F8 gene of Iranian patients with haemophilia A.Factor VIII gene inversions and polymorphisms in Brazilian patients with haemophilia A: carrier detection and prenatal diagnosis.Female monozygotic twins discordant for hemophilia A due to nonrandom X-chromosome inactivation.Familial nonrandom inactivation linked to the X inactivation centre in heterozygotes manifesting haemophilia A.
P2860
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P2860
Severe haemophilia A in a female: a compound heterozygote with nonrandom X-inactivation.
description
1999 nî lūn-bûn
@nan
1999年の論文
@ja
1999年学术文章
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1999年学术文章
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1999年学术文章
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1999年学术文章
@zh-hans
1999年学术文章
@zh-my
1999年学术文章
@zh-sg
1999年學術文章
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1999年學術文章
@zh-hant
name
Severe haemophilia A in a female: a compound heterozygote with nonrandom X-inactivation.
@en
Severe haemophilia A in a female: a compound heterozygote with nonrandom X-inactivation.
@nl
type
label
Severe haemophilia A in a female: a compound heterozygote with nonrandom X-inactivation.
@en
Severe haemophilia A in a female: a compound heterozygote with nonrandom X-inactivation.
@nl
prefLabel
Severe haemophilia A in a female: a compound heterozygote with nonrandom X-inactivation.
@en
Severe haemophilia A in a female: a compound heterozygote with nonrandom X-inactivation.
@nl
P2093
P2860
P1433
P1476
Severe haemophilia A in a female: a compound heterozygote with nonrandom X-inactivation.
@en
P2093
Bassett LM
Gilbert JB
Michaelis RC
Vnencak-Jones CL
P2860
P304
P356
10.1046/J.1365-2516.1999.00352.X
P577
1999-11-01T00:00:00Z