Results 181 to 190 of about 1,101,867 (409)

BIO POSTS: TOOTH FOR TOOTH.

open access: yesInternational Journal of Advanced Research, 2017
Siddharth Kumar   +3 more
openaire   +2 more sources

TBX3‐ Related Disorder

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Heterozygous pathogenic variants in TBX3 cause Ulnar‐Mammary syndrome (UMS). The phenotype is classically characterized by upper limb defects, apocrine/mammary gland hypoplasia, hypogonadism, and various midline defects. However, the clinical spectrum is highly variable, and some individuals may present with a mild or atypical presentation ...
Ziv Halperin, Karin Weiss
wiley   +1 more source

TOOTH GERM CYSTS OF THE JAW [PDF]

open access: green, 1916
Michael G. Wohl
openalex   +1 more source

Hidden Markov random field and FRAME modelling for TCA-image analysis [PDF]

open access: yes
Tooth Cementum Annulation (TCA) is an age estimation method carried out on thin cross sections of the root of human teeth. Age is computed by adding the tooth eruption age to the count of annual incremental lines that are called tooth rings and appear in
Francesco Lagona, Katy Streso
core  

De Novo Heterozygous ZFX Frameshift Variant in a Female With an X‐Linked Neurodevelopmental Disorder

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Germline ZFX variants are associated with an X‐linked neurodevelopmental disorder, with 14 males and 16 females reported to date. We describe a 20‐year‐old female with a heterozygous ZFX frameshift variant, p.(Met666Valfs*2), identified by genome sequencing, previously reported in an affected male.
Iftekhar A. Showpnil   +8 more
wiley   +1 more source

Diagenesis of archaeological bone and tooth

open access: yes, 2018
C. Kendall   +4 more
semanticscholar   +1 more source

Biallelic Variants in the DARS2 Gene as a Novel Cause of Axonal Charcot–Marie–Tooth Disease

open access: yesAnnals of Neurology, EarlyView.
Objective Charcot–Marie–Tooth (CMT) disease is a heterogeneous group of genetic neuropathies, with >90 genes identified. Several aminoacyl‐tRNA synthetases have been linked to CMT. DARS2, encoding the mitochondrial aspartyl‐tRNA synthetase, has been typically associated with leukoencephalopathy with brainstem and spinal cord involvement and lactate ...
Berta Estévez‐Arias   +23 more
wiley   +1 more source

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