The Brain-Lung-Thyroid syndrome (BLTS): A novel deletion in chromosome 14q13.2-q21.1 expands the phenotype to humoral immunodeficiency. (Record no. 28119585)

MARC details
000 -LEADER
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.