Results 221 to 230 of about 288,749 (359)

Differentiating the Clinical and Variant Spectrum of Hardikar Syndrome From Other MED12‐Related Developmental Disorders

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
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

35 Individuals With HUWE1‐Related Neurodevelopmental Disorder and Suggested Clinical Evaluations

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
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

Effectiveness, safety and cost - effectiveness of neonatal screening for familial hypercholesterolemia

open access: green
C Valcalcer Nazco   +1 more
openalex   +1 more source

Proposal for adjustment of the reference values of the basic panel of Neonatal Screening in a hospital in Guatemala. [PDF]

open access: bronze
Pablo Alfonso Tzorín Velásquez   +3 more
openalex   +1 more source

Cryohydrocytosis: When Cold Breaks the Membrane

open access: yes
American Journal of Hematology, EarlyView.
Athina Ntoumaziou   +5 more
wiley   +1 more source

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