[HTML][HTML] Autism spectrum disorder (ASD) and attention deficit hyperactivity disorder (ADHD) with language impairment accompanied by developmental disability …
S Alenezi, A Alyahya, H Aldhalaan - Cureus, 2021 - ncbi.nlm.nih.gov
Abstract Forkhead box protein 1 (FOXP1)(OMIM: 605515) is located at chromosomal region
3p14. 1, which codes for a transcriptional repressor protein. FOXP1 syndrome …
3p14. 1, which codes for a transcriptional repressor protein. FOXP1 syndrome …
[HTML][HTML] Variantes en el número de copias y consanguinidad parental en neonatos de altura con anomalías congénitas en Perú
HHA Barriga, FC Velásquez, CB Carrillo… - Revista de la …, 2022 - ncbi.nlm.nih.gov
Variantes en el número de copias y consanguinidad parental en neonatos de altura con
anomalías congénitas en Perú - PMC Back to Top Skip to main content NIH NLM Logo Access …
anomalías congénitas en Perú - PMC Back to Top Skip to main content NIH NLM Logo Access …
Prenatal diagnosis and counseling of fetal chromosomes with structural abnormalities
G Lv, Y Liu, X Sun, K Mu - 2024 - researchsquare.com
Objectives To explore the pregnancy, fertility risk and genetic suggestions of pregnant
women with complex structural abnormalities of fetal chromosomes. Study Design Amniotic …
women with complex structural abnormalities of fetal chromosomes. Study Design Amniotic …
Copy number variation and parental consanguinity elevated in newborns of high altitude with major congenital anomalies in Perú
AB HH, C Velásquez, B Carrillo, P Tacuri… - Revista de la …, 2022 - europepmc.org
[Copy number variation and parental consanguinity elevated in newborns of high altitude with
major congenital anomalies in Perú]. - Abstract - Europe PMC Sign in | Create an account …
major congenital anomalies in Perú]. - Abstract - Europe PMC Sign in | Create an account …
[HTML][HTML] Variantes en el número de copias y consanguinidad parental elevada en neonatos de altura con anomalías congénitas en Perú Copy number variation and …
HH Abarca-Barriga, FC Velásquez, C Barletta-Carrillo… - revistas.unc.edu.ar
Introducción. Las anomalías congénitas se pueden ocasionar por variantes en el número de
copias o variantes homocigotas heredadas de padres consanguineos. Objetivo. Determinar …
copias o variantes homocigotas heredadas de padres consanguineos. Objetivo. Determinar …