Search Results - "genetic testing"

Risk factors for the progression from acute recurrent to chronic pancreatitis among children in China by Jingqing Zeng, Jiayu Zhang, Yabin Hu, Xiumin Wang, Zhaohui Deng

Connect to this object online.

Previously reported and here added cases demonstrate euploid pregnancies followed by PGT-A as "mosaic" as well as "aneuploid" designated embryos by Norbert Gleicher, Pasquale Patrizio, Lyka Mochizuki, David H. Barad

Connect to this object online.

AMH independently predicts aneuploidy but not live birth per transfer in IVF PGT-A cycles by Howard J. Li, David B. Seifer, Reshef Tal

Connect to this object online.

Mammographies The Cultural Discourses of Breast Cancer Narratives by DeShazer, Mary K.

DOAB: download the publication
DOAB: description of the publication

GENETIC ASPECTS OF INDIRECT HYPERBILIRUBINAEMIA IN NEWBORNS by Katja Jarc Georgiev, Manca Velkavrh

Connect to this object online.

Glycine encephalopathy in newborns and young children: global management standards and a clinical case by M.A. Gonchar, O.L. Logvinova, E.M. Pushkar, O.P. Pomazunovskaya, D.A. Ivakhnenko

Connect to this object online.

Neurofibromatosis type I: points to be considered by general pediatricians by Eungu Kang, Hee Mang Yoon, Beom Hee Lee

Connect to this object online.

Changes to the Employers' Use of Genetic Information and Non-discrimination for Health Insurance in the USA: Implications for Australians by Gemma A. Bilkey, Gareth Baynam, Gareth Baynam, Gareth Baynam, Gareth Baynam, Gareth Baynam, Gareth Baynam, Gareth Baynam, Caron Molster

Connect to this object online.

Prenatal Diagnosis of Atrioventricular Block and QT Interval Prolongation by Fetal Magnetocardiography in a Fetus with Trisomy 18 and SCN5A R1193Q Variant by Lisheng Lin, Miho Takahashi-Igari, Yoshiaki Kato, Yoshihiro Nozaki, Mana Obata, Hiromi Hamada, Hitoshi Horigome

Connect to this object online.

A 16-Day-Old Infant with a Clinical Diagnosis of Classical Cornelia de Lange Syndrome by Pamela Rodríguez, Karla Asturias

Connect to this object online.

ESC National Societies Cardiovascular Journals Editors' Network Almanac 2014: cardiomyopathies by Oliver P. Guttmann, Saidi A. Mohiddin, Perry M. Elliott

Connect to this object online.

CLINICAL FEATURES AND DIAGNOSTIC ALGORITHMS OF CARDIOMYOPATHIES WITH RESTRICTIVE PHENOTYPE CAUSED BY CARDIAC TROPONIN I AND DESMIN GENES MUTATIONS by M.V. Tural'chuk, G.A. Novik, A.Ya. Gudkova

Connect to this object online.

Postpartum multiple vertebral fractures in a patient with osteogenesis imperfecta type I: A case report and literature review by Yumiko Miyazaki, Mizuki Hosokawa, Sho Kudo, Toshimichi Onuma, Makoto Orisaka, Yoshio Yoshida

Connect to this object online.

Value of Gene Polymorphism in the Development of Allergic Disease in Children by T.E. Shumna, S.V. Soloviova, T.P. Zinchenko, V.I. Mazur

Connect to this object online.

Preterm prelabor rupture of membranes after first-trimester chorionic villus sampling: A case report and review of the literature by Jacqueline Early, Pedro Arrabal

Connect to this object online.

Pancreatic cancer - diagnosis, risk factors and treatment. Literature review by Krzysztof Olczyk

Connect to this object online.

Ectodermal dysplasias by Ana L. João, Sofia Antunes-Duarte, Ana Cordeiro, Maria J. Paiva-Lopes

Connect to this object online.

Snyder-Robinson syndrome by Rachel Starks, Patricia Kirby, Michael Ciliberto, Marco Hefti

Connect to this object online.

CLINICAL FEATURES AND DIAGNOSTIC ALGORITHMS OF CARDIOMYOPATHIES WITH RESTRICTIVE PHENOTYPE CAUSED BY CARDIAC TROPONIN I AND DESMIN GENES MUTATIONS by M.V. Tural'chuk, G.A. Novik, A.Ya. Gudkova

Connect to this object online.

Current situation and prospect for the diagnosis and treatment of pediatric critical rare diseases in China by Yingchao Liu, Suyun Qian

Connect to this object online.