Results 111 to 120 of about 3,140 (187)

Duplicação 22q11.2 e defeitos cardíacos congênitos Duplicación 22q11.2 y defectos cardíacos congénitos 22q11.2 duplication and congenital heart defects

Arquivos Brasileiros de Cardiologia, 2009
Rafael Fabiano Machado Rosa, Paulo Ricardo Gazzola Zen, Cláudia Pires Ricachinevsky, Carlo Benatti Pilla, Vera Lúcia Berenstein Pereira, Tatiana Roman, Marilela Varella-Garcia, Giorgio Adriano Paskulin   +7 more
doaj   +1 more source

Spanish translation of the International Glossary on Infertility and Fertility Care, 2017. [PDF]

JBRA Assist Reprod, 2023
Herrero MB, Marín-Briggiler CI, Alaluf MG, Martinez G, Estofan GM.   +4 more
europepmc   +1 more source

Implementación del ADN libre circulante para la detección de aneuploidías fetales. [PDF]

Adv Lab Med
Madrigal Bajo I, Jodar Bifet M, Badenas Orquin C.   +2 more
europepmc   +1 more source

[Sirenomelia: a case report]. [PDF]

Rev Med Inst Mex Seguro Soc
Rodríguez-Partida CE, Gutiérrez-Gómez II.   +1 more
europepmc   +1 more source

Fertilidade na Síndrome de Turner [PDF]

, 2015
Catarina Ribeiro Costa
core  

Brazilian Position Statement for Familial Chylomicronemia Syndrome - 2023. [PDF]

Arq Bras Cardiol, 2023
Izar MCO, Santos Filho RDD, Assad MHV, Chagas ACP, Toledo Júnior AO, Nogueira ACC, Souto ACCF, Lottenberg AMP, Chacra APM, Ferreira CEDS, Lourenço CM, Valerio CM, Cintra DE, Fonseca FAH, Campana GA, Bianco HT, Lima JG, Castelo MHCG, Scartezini M, Moretti MA, Barreto NSF, Maia RE, Montenegro Junior RM, Alves RJ, Figueiredo RMM, Fock RA, Martinez TLDR.   +26 more
europepmc   +1 more source

Hipertricosis localizada y mosaicismo pigmentario tipo Ito (hipomelanosis de Ito)

Anales de Pediatría, 2008
B. Monteagudo Sánchez, E. León Muiños, M. Cabanillas González, G. Martínez Meléndez   +3 more
openaire   +1 more source

Craniofacial abnormalities among patients with Edwards Syndrome. [PDF]

Rev Paul Pediatr, 2013
Rosa RF, Rosa RC, Lorenzen MB, Zen PR, Graziadio C, Paskulin GA.   +5 more
europepmc   +1 more source

[Partial trisomy 9p syndrome: Expanding the phenotype]. [PDF]

Rev Med Inst Mex Seguro Soc
Pérez-Castillo JA, Reyes-Rosales M, Cardoso-Enciso HR, Rodríguez-Cuevas JL.   +3 more
europepmc   +1 more source

[Prevalence of Y-chromosome sequences and gonadoblastoma in Turner syndrome]. [PDF]

Rev Paul Pediatr, 2016
de Marqui AB, da Silva-Grecco RL, Balarin MA.   +2 more
europepmc   +1 more source