Results 221 to 230 of about 25,055 (273)

Clonal-aggregative multicellularity tuned by salinity in a choanoflagellate. [PDF]

open access: yesNature
Ros-Rocher N   +10 more
europepmc   +1 more source

Refining Domain‐Based Prognostication in DNM1 Encephalopathy: A Mild Phenotype Associated With a GTPase Domain Variant

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT DNM1 encephalopathy is a rare autosomal dominant genetic condition characterized by a range of neurological and developmental manifestations. The typical phenotype is severe, including profound intellectual disability, treatment‐resistant epilepsy, ataxia, and structural brain abnormalities. However, milder presentations have increasingly been
Caroline Crain   +6 more
wiley   +1 more source

Toward equitable and evidence-based care in Hereditary Angioedema: Time for inclusive global guidelines. [PDF]

open access: yesWorld Allergy Organ J
Morais-Almeida M   +6 more
europepmc   +1 more source

First National Expanded Genomic Newborn Screening Program in Qatar; A Pilot Study, Doha‐Heidelberg Collaboration

open access: yes
American Journal of Medical Genetics Part A, EarlyView.
Reem Alsulaiman   +18 more
wiley   +1 more source
Some of the next articles are maybe not open access.

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Odor signatures and kin recognition

Physiology and Behavior, 1985
The basis of olfactory signatures mediating human kin recognition was investigated in two experiments. The odors of mothers and offspring were correctly matched (by subjects unfamiliar with the stimulus individuals) at a greater than chance frequency. In contrast, subjects were not able reliably to match the odors of husbands and wives.
Richard H Porter
exaly   +3 more sources

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