The Brain-Lung-Thyroid syndrome (BLTS): A novel deletion in chromosome 14q13.2-q21.1 expands the phenotype to humoral immunodeficiency. (Record no. 28119585)
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000 -LEADER | |
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fixed length control field | 01600 a2200445 4500 |
005 - DATE AND TIME OF LATEST TRANSACTION | |
control field | 20250517202809.0 |
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION | |
fixed length control field | 201810s 0 0 eng d |
022 ## - INTERNATIONAL STANDARD SERIAL NUMBER | |
International Standard Serial Number | 1878-0849 |
024 7# - OTHER STANDARD IDENTIFIER | |
Standard number or code | 10.1016/j.ejmg.2018.02.007 |
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 | Villafuerte, Beatriz |
264 #0 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE | |
Date of production, publication, distribution, manufacture, or copyright notice | 20181010 |
245 00 - TITLE STATEMENT | |
Title | The Brain-Lung-Thyroid syndrome (BLTS): A novel deletion in chromosome 14q13.2-q21.1 expands the phenotype to humoral immunodeficiency. |
Medium | [electronic resource] |
260 ## - PUBLICATION, DISTRIBUTION, ETC. | |
Name of publisher, distributor, etc. | European journal of medical genetics |
Date of publication, distribution, etc. | Jul 2018 |
300 ## - PHYSICAL DESCRIPTION | |
Extent | 393-398 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 | Athetosis |
General subdivision | genetics |
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
Topical term or geographic name entry element | Child |
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
Topical term or geographic name entry element | Chorea |
General subdivision | genetics |
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
Topical term or geographic name entry element | Chromosome Deletion |
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
Topical term or geographic name entry element | Chromosomes, Human, Pair 14 |
General subdivision | genetics |
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
Topical term or geographic name entry element | Congenital Hypothyroidism |
General subdivision | genetics |
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 | Humans |
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
Topical term or geographic name entry element | Immunologic Deficiency Syndromes |
General subdivision | genetics |
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
Topical term or geographic name entry element | Phenotype |
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
Topical term or geographic name entry element | Respiratory Distress Syndrome, Newborn |
General subdivision | genetics |
700 1# - ADDED ENTRY--PERSONAL NAME | |
Personal name | Natera-de-Benito, Daniel |
700 1# - ADDED ENTRY--PERSONAL NAME | |
Personal name | González, Aidy |
700 1# - ADDED ENTRY--PERSONAL NAME | |
Personal name | Mori, María A |
700 1# - ADDED ENTRY--PERSONAL NAME | |
Personal name | Palomares, María |
700 1# - ADDED ENTRY--PERSONAL NAME | |
Personal name | Nevado, Julián |
700 1# - ADDED ENTRY--PERSONAL NAME | |
Personal name | García-Miñaur, Sixto |
700 1# - ADDED ENTRY--PERSONAL NAME | |
Personal name | Lapunzina, Pablo |
700 1# - ADDED ENTRY--PERSONAL NAME | |
Personal name | González-Granado, Luis I |
700 1# - ADDED ENTRY--PERSONAL NAME | |
Personal name | Allende, Luis M |
700 1# - ADDED ENTRY--PERSONAL NAME | |
Personal name | Moreno, José C |
773 0# - HOST ITEM ENTRY | |
Title | European journal of medical genetics |
Related parts | vol. 61 |
-- | no. 7 |
-- | p. 393-398 |
856 40 - ELECTRONIC LOCATION AND ACCESS | |
Uniform Resource Identifier | <a href="https://doi.org/10.1016/j.ejmg.2018.02.007">https://doi.org/10.1016/j.ejmg.2018.02.007</a> |
Public note | Available from publisher's website |
No items available.