Results 231 to 240 of about 311,384 (302)

Expanding the Evaluation of Skeletal Anomalies in Patients With KBG Syndrome: Recommendations for Clinical Practice

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT KBG syndrome is a rare autosomal dominant neurodevelopmental disorder caused by ANKRD11 haploinsufficiency and is characterized by short stature, distinctive facial features, intellectual disability or developmental delay, congenital anomalies and skeletal anomalies.
Marit van der Leij   +5 more
wiley   +1 more source

Enhancing Perinatal Care for Women With Intellectual Disabilities: Clinician Insights on Involving Family Caregivers. [PDF]

open access: yesJ Appl Res Intellect Disabil
Smith LD   +6 more
europepmc   +1 more source

'Give People More Time and Take the Time to Explain Things Properly': Cervical Screening Experiences of People With Intellectual Disability. [PDF]

open access: yesJ Appl Res Intellect Disabil
Strnadová I   +7 more
europepmc   +1 more source

Clinical Diagnostics After Failed Hearing Screening in People With Intellectual Disabilities Do Not Often Take Place. [PDF]

open access: yesJ Intellect Disabil Res
Wiegand A   +22 more
europepmc   +1 more source

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