Results 111 to 120 of about 2,841 (212)
Clinical molecular genetics in the UK c.1975-c.2000 [PDF]
, 2014 seminar transcriptChaired by Professor Martin Bobrow and introduced by Professor Bob Williamson, this Witness Seminar included geneticists from a broad range of research and clinical specialities.
Jones, EM, Tansey, EM
core
Rare Pediatric Genetic Case Report of X-linked Hypohidrotic Ectodermal Dysplasia Type 1. [PDF]
Cureus, 2023 Zaki H.
europepmc +1 more source
Need for Animal Models of Meibomian Gland Dysfunction [PDF]
, 2016 Louis Tong, Preeya. K. Gupta
core +1 more source
Hypohidrotic Ectodermal Dysplasia [PDF]
, 2020 ELBEK ÇUBUKÇU, ÇİĞDEM +2 more
openaire +3 more sources
Molecular basis and genetics of hypohidrotic ectodermal dysplasias. [PDF]
Vavilovskii Zhurnal Genet Selektsii, 2023 Kovalskaia VA +3 more
europepmc +1 more source
Ectodermal dysplasia: A report of two cases
Journal of Craniomaxillofacial Research, 2017 Introduction: Ectodermal dysplasia (ED) is a group of syndromes and disorders in the human body characterized by structural anomalies in the ectoderm and often associated with hair, teeth and skin abnormalities.
Mozhgan Kazemian +2 more
doaj
Unexplained Fever in Infancy: Report of a Rare Case of Hypohidrotic Ectodermal Dysplasia in an Infant. [PDF]
Cureus, 2023 Gilitwala ZS, Satpute SR.
europepmc +1 more source
Hypohidrotic ectodermal dysplasia
Journal of the Pediatrics Association of India, 2013 Ratna Yumkham +3 more
openaire +1 more source
A case study of a novel homozygous EDAR splice site variant in hypohidrotic ectodermal dysplasia with tooth agenesis: molecular dynamics insights. [PDF]
BMC Med GenomicsNejati P +3 more
europepmc +1 more source