Library collection
Database :
article
Search on :
HAZAN, FILIZ [Author]
References found :
3
[
refine
]
Displaying:
1 .. 3
in format [
ISO 690
]
page 1 of 1
1 / 3
select
to print
Katipoğlu, Nagehan et al.
Síndrome de anemia megaloblástica sensible a la tiamina de aparición en la niñez, con mutación en el genSLC19A2: caso clínico
.
Arch. argent. pediatr.
, Jun 2017, vol.115, no.3, p.e153-e156. ISSN 0325-0075
·
abstract in spanish
|
english
·
text in spanish
2 / 3
select
to print
Hazan, Filiz et al.
Niño con síndrome tricorrinofalángico tipo II acompañado de baja estatura
.
Arch. argent. pediatr.
, Dic 2016, vol.114, no.6, p.e403-e407. ISSN 0325-0075
·
abstract in spanish
|
english
·
text in spanish
3 / 3
select
to print
Korkmaz, Hüseyin A et al.
Asociación entre el síndrome de Wolfram y la tetralogía de Fallot en una niña
.
Arch. argent. pediatr.
, Jun 2016, vol.114, no.3, p.e163-e166. ISSN 0325-0075
·
abstract in spanish
|
english
·
text in spanish
page 1 of 1
Refine the search
Database :
article
Advanced form
Search for :
Free form
Basic form
Search
in field
1
All indexes
Title words
Author
Clinical Trials Registry
Subject
Abstract
Publication year
Article type
Affiliation - Organization
Affiliation - Country, Country
2
and
or
and not
All indexes
Title words
Author
Clinical Trials Registry
Subject
Abstract
Publication year
Article type
Affiliation - Organization
Affiliation - Country, Country
3
and
or
and not
All indexes
Title words
Author
Clinical Trials Registry
Subject
Abstract
Publication year
Article type
Affiliation - Organization
Affiliation - Country, Country
Search engine:
iAH
powered by
WWWISIS
BIREME/PAHO/WHO - Latin American and Caribbean Center on Health Sciences Information
