Results 111 to 120 of about 1,837 (195)

A new frontonasal dysplasia syndrome associated with deletion of the SIX2 gene. [PDF]

open access: yesAm J Med Genet A, 2016
Hufnagel RB   +5 more
europepmc   +1 more source

BTB domain mutations perturbing KCTD15 oligomerisation cause a distinctive frontonasal dysplasia syndrome. [PDF]

open access: yesJ Med Genet
Miller KA   +17 more
europepmc   +1 more source

Aristaless-Like Homeobox protein 1 (ALX1) variant associated with craniofacial structure and frontonasal dysplasia in Burmese cats. [PDF]

open access: yesDev Biol, 2016
Lyons LA   +7 more
europepmc   +1 more source

Facial Abnormality (Frontonasal Dysplasia Sequence)

open access: yesPediatric Oncall, 2014
Shweta Anand, Anju Kapoor
openaire   +1 more source

Frontonasal and Frontofacionasal Dysplasias. Case Report

open access: yesSalud Uninorte, 2015
Jenny Ramírez-Gil   +4 more
openaire   +1 more source

A Pattern of Malformations in the First Trimester Ultrasound. [PDF]

open access: yesJ Med Ultrasound
Sereno S   +5 more
europepmc   +1 more source

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