✦ LIBER ✦

Characterization of molecular defects of hemophilia B in Taiwan

✍ Scribed by S.W. Lin; M.C. Shen

Book ID: 119038188
Publisher: Elsevier Science
Year: 1991
Tongue: English
Weight: 94 KB
Volume: 63
Category: Article
ISSN: 0049-3848
DOI: 10.1016/0049-3848(91)90297-a

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Characterization of genetic defects of h

Characterization of genetic defects of hemophilia A in mainland China

✍ Y.Z. Zhang; J.X. Liu; H.Z. Shao; Z.W. Chi; H.L. Wang; S.J. Chen; Z. Chen; Z.Y. W 📂 Article 📅 1999 🏛 Elsevier Science 🌐 English ⚖ 58 KB

The Molecular Genetics of Hemophilia B

✍ Valerie A. Geddes; Ross T.A. MacGillivray 📂 Article 📅 1987 🏛 Elsevier Science 🌐 English ⚖ 1005 KB

Prenatal and molecular diagnosis of hemo

Prenatal and molecular diagnosis of hemophilia B

✍ Young, Ji-Hsiung; Wang, Jyh-Chwan; Gau, Jyh-Pyng; Hu, Han-Tien 📂 Article 📅 1996 🏛 John Wiley and Sons 🌐 English ⚖ 589 KB

Prenatal diagnosis was carried out on a woman who had previously given birth to a son with a spontaneous mutation of C + T transition at nt 31133 of the factor IX (F.IX) gene. The diagnosis was performed on chorionic villi sampling by the method of amplificationcreated restriction site (ACRS). It re

In vitro Cytokine Treatment of B Cell De

In vitro Cytokine Treatment of B Cell Defects in HIV-Infected Hemophilia Patients

✍ Rolf Weimer; Silvia Zipperle; Volker Daniel; Gerhard Opelz 📂 Article 📅 1995 🏛 John Wiley and Sons 🌐 English ⚖ 743 KB

Frequency of congenital heart defects in

Frequency of congenital heart defects in patients with hemophilia

✍ Jedele, Kerry B. ;Michels, Virginia V. ;Gordon, Hymie ;Gilchrist, Gerald S. 📂 Article 📅 1990 🏛 John Wiley and Sons 🌐 English ⚖ 365 KB 👁 2 views

Spectrum of molecular defects and mutati

Spectrum of molecular defects and mutation detection rate in patients with severe hemophilia A

✍ Nadja Bogdanova; Arseni Markoff; Hartmut Pollmann; Ulrike Nowak-Göttl; Roswith E 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 English ⚖ 168 KB

Hemophilia A is the most frequently occurring X-linked bleeding disorder, affecting one to two out of 10,000 males worldwide. Various types of mutations in the F8 gene are causative for this condition. It is well known that the most common mutation in severely affected patients is the intron 22 inve