Congenital deficiency of factor XIII caused by two missense mutations in a Dutch family. (Record no. 15765224)
[ view plain ]
| 000 -LEADER | |
|---|---|
| fixed length control field | 01452 a2200433 4500 |
| 005 - DATE AND TIME OF LATEST TRANSACTION | |
| control field | 20250515000521.0 |
| 008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION | |
| fixed length control field | 200611s 0 0 eng d |
| 022 ## - INTERNATIONAL STANDARD SERIAL NUMBER | |
| International Standard Serial Number | 1351-8216 |
| 024 7# - OTHER STANDARD IDENTIFIER | |
| Standard number or code | 10.1111/j.1365-2516.2005.01137.x |
| Source of number or code | doi |
| 040 ## - CATALOGING SOURCE | |
| Original cataloging agency | NLM |
| Language of cataloging | eng |
| Transcribing agency | NLM |
| 100 1# - MAIN ENTRY--PERSONAL NAME | |
| Personal name | Onland, W |
| 264 #0 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE | |
| Date of production, publication, distribution, manufacture, or copyright notice | 20061108 |
| 245 00 - TITLE STATEMENT | |
| Title | Congenital deficiency of factor XIII caused by two missense mutations in a Dutch family. |
| Medium | [electronic resource] |
| 260 ## - PUBLICATION, DISTRIBUTION, ETC. | |
| Name of publisher, distributor, etc. | Haemophilia : the official journal of the World Federation of Hemophilia |
| Date of publication, distribution, etc. | Sep 2005 |
| 300 ## - PHYSICAL DESCRIPTION | |
| Extent | 539-47 p. |
| Other physical details | digital |
| 500 ## - GENERAL NOTE | |
| General note | Publication Type: Case Reports; Journal Article |
| 650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
| Topical term or geographic name entry element | Adult |
| 650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
| Topical term or geographic name entry element | Child, Preschool |
| 650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
| Topical term or geographic name entry element | DNA Mutational Analysis |
| 650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
| Topical term or geographic name entry element | Factor XIII |
| General subdivision | genetics |
| 650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
| Topical term or geographic name entry element | Factor XIII Deficiency |
| General subdivision | congenital |
| 650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
| Topical term or geographic name entry element | Female |
| 650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
| Topical term or geographic name entry element | Hemorrhage |
| General subdivision | etiology |
| 650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
| Topical term or geographic name entry element | Humans |
| 650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
| Topical term or geographic name entry element | Infant, Newborn |
| 650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
| Topical term or geographic name entry element | Male |
| 650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
| Topical term or geographic name entry element | Mutation, Missense |
| 650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
| Topical term or geographic name entry element | Pedigree |
| 650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
| Topical term or geographic name entry element | Umbilical Cord |
| 700 1# - ADDED ENTRY--PERSONAL NAME | |
| Personal name | Böing, A N |
| 700 1# - ADDED ENTRY--PERSONAL NAME | |
| Personal name | Meijer, A B |
| 700 1# - ADDED ENTRY--PERSONAL NAME | |
| Personal name | Schaap, M C L |
| 700 1# - ADDED ENTRY--PERSONAL NAME | |
| Personal name | Nieuwland, R |
| 700 1# - ADDED ENTRY--PERSONAL NAME | |
| Personal name | Haasnoot, K |
| 700 1# - ADDED ENTRY--PERSONAL NAME | |
| Personal name | Sturk, A |
| 700 1# - ADDED ENTRY--PERSONAL NAME | |
| Personal name | Peters, M |
| 773 0# - HOST ITEM ENTRY | |
| Title | Haemophilia : the official journal of the World Federation of Hemophilia |
| Related parts | vol. 11 |
| -- | no. 5 |
| -- | p. 539-47 |
| 856 40 - ELECTRONIC LOCATION AND ACCESS | |
| Uniform Resource Identifier | <a href="https://doi.org/10.1111/j.1365-2516.2005.01137.x">https://doi.org/10.1111/j.1365-2516.2005.01137.x</a> |
| Public note | Available from publisher's website |
No items available.