Results 151 to 160 of about 609,557 (305)

A Population‐Based Assessment of Cancer Risk in Children With VACTERL

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Cancer risk in children with VACTERL, a nonrandom co‐occurrence of ≥ 3 defects (vertebral, anal, cardiac, tracheoesophogeal fistula, renal, and limb), remains unclear. We evaluated this association in a population‐based study. We analyzed data from the Genetic Overlap Between Anomalies and Cancer in Kids (GOBACK) Study, a US registry linkage ...
Ji Yun Tark, Alexander Renwick, Giorgio Tettamanti, Rachel D. Harris, Tania A. Desrosiers, Andrew F. Olshan, Amanda E. Janitz, Michael E. Scheurer, Charles J. Shumate, Angela E. Scheuerle, Sharon E. Plon, Chad D. Huff, Ann Nordgren, Barbara Luke, Philip J. Lupo, Jeremy M. Schraw   +15 more
wiley   +1 more source

Exploring GBA1 gene in Parkinson's disease: Prevalence and variant spectrum from Asia minor. [PDF]

Neurol Sci
Koç Yekedüz M, Yilmaz R, Abali T, Kibrit SN, Karacan AV, Unutmaz EY, Ayık G, Genç-Batmaz D, Dilek GR, Çelik B, Gemci E, Şahin T, Yalcin A, Ceylaner S, Akbostancı MC, Eminoğlu FT.   +15 more
europepmc   +1 more source

Diversity of spined loaches from Asia Minor in a phylogenetic context (Teleostei: Cobitidae). [PDF]

PLoS One, 2018
Perdices A, Ozeren CS, Erkakan F, Freyhof J.   +3 more
europepmc   +1 more source

The Community That Raymond Brown Left Behind: Reflections on the Johannine Dialectical Situation

, 2013
Among the paradigm-making contributions in Johannine studies over the last half century, one of the most significant is the sketching of “the community of the Beloved Disciple” by Raymond E. Brown (Brown 1979). Extending beyond Johannine studies, Brown’s
Anderson, Paul N.
core  

Noonan Syndrome Spectrum Disorders Predispose to Systemic Lupus Erythematosus: Case Report and Critical Review of the Literature

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT RASopathies are clinically overlapping neurodevelopmental syndromes resulting from germline mutations in genes involved in the rat sarcoma/mitogen‐activated protein kinases (RAS/MAPK) pathway. Historically, RASopathies have been described by clinical phenotypes, such as Noonan syndrome and Neurofibromatosis type I.
Anastasia‐Vasiliki Madenidou, Gillian I. Rice, James O'Sullivan, Ben Parker, Ian N. Bruce, Emma Burkitt‐Wright, Tracy A. Briggs   +6 more
wiley   +1 more source

Mitochondrial Phylogeography of Wild Boars, <i>Sus scrofa</i>, from Asia Minor: Endemic Lineages, Natural Immigration, Historical Anthropogenic Translocations, and Possible Introgression of Domestic Pigs. [PDF]

Animals (Basel)
Demirbaş Y, Soysal H, Koca AÖ, Stefanović M, Suchentrunk F.   +4 more
europepmc   +1 more source

Recent discovery of phallic depictions in prehistoric cave art in Asia Minor. [PDF]

Turk J Urol, 2017
Verit A.
europepmc   +1 more source

Clitic doubling from Ancient to Asia Minor Greek [PDF]

, 2008
Janse, Mark
core  

Marfan Syndrome Associated With Intellectual Disability and Behavioral Anomalies: Further Evidence for the Effect of Compound Heterozygous Variants in FBN1 on Phenotypic Severity

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Marfan syndrome (MFS) is a rare connective tissue disorder characterized by involvement of the cardiovascular, ocular, and musculoskeletal systems. Pathogenic variants in FBN1 cause most of the MFS cases; however, intellectual disability (ID) is rarely observed. A non‐consanguineous Pakistani family with four affected individuals was recruited.
Azmatullah Khan, Naseebullah Kakar, Ainullah Kakar, Malte Spielmann, Sajid Malik   +4 more
wiley   +1 more source

Evaluation of Biopesticides for Management of Bemisia tabaci Middle East-Asia Minor 1 (Hemiptera: Aleyrodidae) in Florida. [PDF]

Insects
Dimase M, Lahiri S, Beuzelin J, Hutton S, Smith HA.   +4 more
europepmc   +1 more source