CGH Array and Karyotype as Complementary Tools in Prenatal Diagnosis: Prenatal Diagnosis of a 4q Derivative Chromosome from Maternal 4q;11q Translocation-Reference-Cited by-同舟云学术

CGH Array and Karyotype as Complementary Tools in Prenatal Diagnosis: Prenatal Diagnosis of a 4q Derivative Chromosome from Maternal 4q;11q Translocation

Published:2018-05-04 Issue:3 Volume:37 Page:184-190
ISSN:1551-3815
Container-title:Fetal and Pediatric Pathology
language:en
Short-container-title:Fetal and Pediatric Pathology

Author:

Gonzalez Cristina¹,Serrano Miriam Gutierrez¹,Barbancho Lopez Carmen²,Garcia-Riaño Taida²,Barea Calero Vanesa¹,Moreno Perea Rebeca¹,Rodriguez Mogollón Begoña¹,Queipo Rojas Amelia¹,Climent Ana Garcia³,Cava Valenciano Fernando⁴

Affiliation:

1. Genetics Department, Hospital Universitario Infanta Sofia, San Sebastian de los Reyes, Madrid, Spain

2. Gynecology and Obstretics Department, Hospital Universitario Infanta Sofia, San Sebastian de los Reyes, Madrid, Spain

3. CIALAB, Genetics, Calle Cristo de la Paz, San Juan de Alicante, Alicante, Spain

4. Clinical Laboratory, Hospital Universitario Infanta Sofia, San Sebastian de los Reyes, Madrid, Spain

Publisher

Informa UK Limited

Subject

General Medicine,Pathology and Forensic Medicine,Pediatrics, Perinatology and Child Health

Link

https://www.tandfonline.com/doi/pdf/10.1080/15513815.2018.1467518

Reference15 articles.

1. Prevalence of congenital anomalies in five British regions, 1991-99

2. Accuracy of Ultrasonography at 11–14 Weeks of Gestation for Detection of Fetal Structural Anomalies

3. Clinical utility of array comparative genomic hybridisation for prenatal diagnosis: a cohort study of 3171 pregnancies

4. Resolving the resolution of array CGH

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3. Prenatal Diagnosis of 4q Terminal Deletion and Review of the Literature;Cytogenetic and Genome Research;2019