Results 51 to 60 of about 376 (181)

Prenatal Diagnosis of Pfeiffer Syndrome Patient with FGFR2 C.940-1G>C Variant: A Case Report. [PDF]

open access: yesAppl Clin Genet, 2020
Torres-Canchala L   +5 more
europepmc   +1 more source

Differential diagnosis of syndromic craniosynostosis: a case series. [PDF]

open access: yesArch Gynecol Obstet, 2022
Casteleyn T   +4 more
europepmc   +1 more source

Greig Cephalopolysyndactyly Contiguous Gene Syndrome: Case Report and Literature Review. [PDF]

open access: yesGenes (Basel), 2021
Kozma K   +13 more
europepmc   +1 more source

Ontology-based methods for disease similarity estimation and drug repositioning [PDF]

open access: yes
Title from PDF of title page, viewed on October 2, 2012Dissertation advisor: Deendayal DinakarpandianVitaIncludes bibliographic references (p. 174-181)Thesis (Ph.D.)--School of Computing and Engineering and Dept. of Mathematics and Statistics. University
Mathur, Sachin
core  

TWIST1, a gene associated with Saethre-Chotzen syndrome, regulates extraocular muscle organization in mouse. [PDF]

open access: yesDev Biol, 2022
Whitman MC   +5 more
europepmc   +1 more source

[Acrocephalosyndactylia syndromes].

open access: yesWiadomosci lekarskie (Warsaw, Poland : 1960), 1980
Z, Kopyść, J, Ryzko, C, Gura
openaire   +3 more sources

Craniofacial morphology in Apert syndrome: a systematic review and meta-analysis. [PDF]

open access: yesSci Rep, 2022
Alam MK   +5 more
europepmc   +1 more source

Clinical Nasal Deviation Following Midface Advancement in Patients With Syndromic Craniosynostosis. [PDF]

open access: yesJ Craniofac Surg
Cuperus IE   +5 more
europepmc   +1 more source

Inference for decorated graphs and application to multiplex networks

open access: yes
A graphon is a limiting object used to describe the behaviour of large networks through a function that captures the probability of edge formation between nodes.
Dufour, Charles, Olhede, Sofia C.
core  

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