Results 91 to 100 of about 59,142 (275)

Haplotype-based associations with relatively major effects (>15%) for the traits of leaf angle (LA), ear height (EH), plant height (PH) and the EH/PH ratio, measured in inbred lines of tropical maize during two growing seasons.

open access: yes, 2019
Haplotype-based associations with relatively major effects (>15%) for the traits of leaf angle (LA), ear height (EH), plant height (PH) and the EH/PH ratio, measured in inbred lines of tropical maize during two growing seasons.
Carlos Maldonado (5527520)   +3 more
core   +1 more source

Expanded Phenotype Associated With an Intronic PPP1R12A Variant: A Case Report and Literature Review

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Autosomal dominant PPP1R12A‐related genitourinary and/or brain malformation syndrome is a recently described multisystem disorder caused by loss‐of‐function variants in the protein phosphatase 1 regulatory subunit 12a (PPP1R12A) gene. To date, 22 affected individuals have been reported with variable brain malformations and genitourinary ...
Emily M. Bland   +4 more
wiley   +1 more source

GWAS results for plant and ear height (cm).

open access: yes, 2015
a The phenotypic observation used for the GWAS was the BLUP for the hybrid effect obtained using model in Eq. (3).b The phenotypic observation used for the GWAS was the BLUP for the hybrid effect from the MET model in Eq.
Pei-Cheng Huang (695985)   +8 more
core   +1 more source

Psychoacoustics of height perception in 3D audio

open access: yes, 2021
Recently developed 3D audio loudspeaker formats employ the so-called “height” channels, utilizing loudspeakers in elevated positions as well as at the ear level.
Hyunkook Lee, Lee, Hyunkook
core   +1 more source

Assessment of Growth in Cardio‐Facio‐Cutaneous Syndrome

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Cardio‐facio‐cutaneous (CFC) syndrome is a rare, multiple congenital anomaly disorder in which individuals commonly experience faltering growth; however, systematic analysis of growth parameters in this disorder has not been performed. We recruited 69 participants with CFC through CFC International and collected data on assessing height ...
Kari Johnston   +6 more
wiley   +1 more source

Genetic Variability and Genotypic, Phenotypic Correlation Studies for Yield and Related Traits In Single Cross Hybrids of Maize (Zea Mays L.)

open access: yesScience Journal of University of Zakho, 2014
The study was connected to evaluate seven mays hybrids for genetic variability for yield components at Faculty of Agriculture and forestry field university of Duhok during spring 2011 and 2012 .The result show highly significant different between the ...
Mohammed O. Mohammed
doaj  

Field Population Density Effects on Field Yield and Morphological Characteristics of Maize

open access: yesAgriculture, 2019
The objective of this study was to evaluate the effect of population density and row spacing on field yield and other morphological characteristics of two commercial F1 maize hybrids of different biological cycle (Costanza and LG3535) in a four-year ...
Vasileios Greveniotis   +3 more
doaj   +1 more source

The Diagnosis That Arrived Decades Late: Living Without and Then With Myhre Syndrome

open access: yesAmerican Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Myhre syndrome (MIM #139210) is a rare multisystem disorder first described in 1981, characterized by short stature, neurodevelopmental delay, joint contractures, and cardiopulmonary complications. Its molecular basis, recurrent pathogenic variants in SMAD4, was not discovered until 2011. This narrative is based on a review of medical records,
Abdallah F. Elias
wiley   +1 more source

Review of the Molecular and Developmental Basis of Myhre Syndrome, Bench Research

open access: yesAmerican Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Myhre syndrome (MS) is a connective‐tissue disorder within the acromelic dysplasia spectrum. It is characterized by congenital craniofacial, skeletal, cutaneous anomalies, respiratory, cardiovascular along with intellectual disability, deafness, and progressive fibrosis.
Camille Viaut, Valerie Cormier‐Daire
wiley   +1 more source

Genome-wide association analysis of plant height and ear height related traits in maize

open access: yesActa Agronomica Sinica, 2023
Ya-Jie MA   +9 more
openaire   +1 more source

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