Results 221 to 230 of about 288,749 (359)
ABSTRACT The rare X‐linked female‐restricted Hardikar syndrome (HDKR, OMIM # 301068) is characterized by multiple congenital anomalies including orofacial clefts, gastrointestinal, genitourinary, and cardiac anomalies, but cognitive and neurobehavioral development is rarely impaired.
Tinne Warmoeskerken +4 more
wiley +1 more source
Ten-Year Anniversary of the <i>International Journal of Neonatal Screening</i>: Revisiting Its Scope. [PDF]
Fingerhut R, Schielen PCJI.
europepmc +1 more source
35 Individuals With HUWE1‐Related Neurodevelopmental Disorder and Suggested Clinical Evaluations
ABSTRACT HUWE1 (HECT, UBA, and WWE Domain Containing E3 Ubiquitin Protein Ligase1, OMIM 300697), located at Xp11.22, encodes a ubiquitin ligase that is highly conserved across species. Genetic variants in HUWE1 described in multiple independent studies cause X‐linked intellectual disability, including in the patients identified by Juberg, Marsidi, and ...
Mindy H. Li +25 more
wiley +1 more source
The lived experience of migrant Syrian mothers' interaction with the neonatal screening program. [PDF]
Sezerol MA, Altaş ZM, Arslan E.
europepmc +1 more source
Economic evaluation of the role of telemedicine in paediatric cardiology: Final Report [PDF]
Dowie, R +3 more
core
Proposal for adjustment of the reference values of the basic panel of Neonatal Screening in a hospital in Guatemala. [PDF]
Pablo Alfonso Tzorín Velásquez +3 more
openalex +1 more source
Cryohydrocytosis: When Cold Breaks the Membrane
American Journal of Hematology, EarlyView.
Athina Ntoumaziou +5 more
wiley +1 more source

