Results 71 to 80 of about 4,166,884 (251)

Speech and Language Disorders Associated With 7q31 Deletions Implicating FOXP2

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Some 7q31 deletions encompass FOXP2, a gene long associated with speech and language disorders. Intragenic pathogenic FOXP2 variants cause FOXP2‐related speech and language disorder, which has been well characterized in the literature. Conversely, the phenotype associated with 7q31 deletions is neglected.
Lottie D. Morison   +3 more
wiley   +1 more source

Bakker and Montesano Montessori (eds.) (2016) Complexity in Education: From Horror to Passion

open access: yesPRISM, 2017
Book ...
Jacqueline Dodding
doaj   +1 more source

Book Review: Beyond Orientalism [PDF]

open access: yes, 2001
A review of Beyond Orientalism by Fred ...
Patton, Laurie
core   +2 more sources

Down Syndrome in Maternity Care: Mothers' Experiences of Prenatal Screening

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Prenatal screening for Down syndrome (DS) is offered to expectant parents receiving antenatal care in many countries, with an emphasis on providing parents with the opportunity to make informed choices about their pregnancy. We examined experiences of prenatal screening among mothers of children with DS living in England, Scotland, or Wales ...
Tamar Rutter   +5 more
wiley   +1 more source

Book Review [PDF]

open access: yes, 2005
Reviewing, Richard A. Posner, Catastrophe: Risk and Response (Oxford University Press, 2004) and Jared Diamond, Collapse: How Societies Choose to Fail or Succeed (Viking ...
Wiener, Jonathan B.
core   +1 more source

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