✦ LIBER ✦

Monitoring for new multiple congenital anomalies in the search for human teratogens

✍ Scribed by Khoury, Muin J. ;Botto, Lorenzo ;Waters, Grady D. ;Mastroiacovo, Pierpaolo ;Castilla, Eduardo ;Erickson, J. David

Publisher: John Wiley and Sons
Year: 1993
Tongue: English
Weight: 667 KB
Volume: 46
Category: Article
ISSN: 0148-7299
DOI: 10.1002/ajmg.1320460425

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

From telomeres to T-antigens: Many roads

From telomeres to T-antigens: Many roads … multiple pathways … novel associations in the search for the origins of human gliomas

✍ Eugene O. Major 📂 Article 📅 2000 🏛 John Wiley and Sons 🌐 English ⚖ 85 KB 👁 3 views

Capillary electrophoresis combined with

Capillary electrophoresis combined with microdialysis in the human spinal cord: A new tool for monitoring rapid peroperative changes in amino acid neurotransmitters within the dorsal horn

✍ Sandrine Parrot; Valérie Sauvinet; Jean-Michel Xavier; Delphine Chavagnac; Laure 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 English ⚖ 119 KB 👁 1 views

Other origins: The search for the giant

Other origins: The search for the giant ape in human prehistory. By Russell Ciochon, John Olsen, and Jamie James. New York: Bantam. xi + 262 pp. $22.95 (cloth)

✍ David J. Daegling 📂 Article 📅 1992 🏛 John Wiley and Sons 🌐 English ⚖ 297 KB

Bones of contention. Controversies in th

Bones of contention. Controversies in the search for human origins. By Roger Lewin. New York: Simon and Schuster. 1987. 348 pp., figures, notes, index. $19.95 (cloth)

✍ Patricia S. Bridges 📂 Article 📅 1988 🏛 John Wiley and Sons 🌐 English ⚖ 213 KB 👁 2 views

The hominid gang. Behind the scenes in t

The hominid gang. Behind the scenes in the search for human origins. By Delta Willis. New York: Viking Penguin Inc. 1989. xii + 352 pp., figures, footnotes, index. $21.95 (cloth)

✍ Sally McBrearty 📂 Article 📅 1991 🏛 John Wiley and Sons 🌐 English ⚖ 206 KB

Search for mutations in a segment of the

Search for mutations in a segment of the exon 28 of the human von Willebrand factor gene: New mutations, R1315C and R1341W, associated with type 2M and 2B variants

✍ Casaña, Pilar; Martínez, Francisco; Espinós, Carmen; Haya, Saturnino; Lorenzo, J 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 431 KB 👁 1 views

von Willebrand Disease (vWD) is the most frequently inherited bleeding disorder in humans, and is caused by a qualitative and/or quantitative abnormality of the von Willebrand factor (vWF). A large number of defects that cause qualitative variants have been located in the A1 domain of the vWF, which