Surgical management of ectrodactyly-associated foot deformity in a child: a case report. [PDF]
Raza S +8 more
europepmc +1 more source
Ectrodactyly, Cleft Lip/Palate, and Urinary Anomalies With a Tumor Protein p63 (TP63) Mutation: A Case Report and Literature Review. [PDF]
Mohamed RH +4 more
europepmc +1 more source
Novel Missense Variant in the FGFR1 Gene Associated With Prenatal Diagnosis of Hartsfield Syndrome. [PDF]
Hodges MB, Gilmore KL, Dyke MJ, Vora NL.
europepmc +1 more source
Confirmation of the Hotspot Variant in <i>MAP3K20</i> Responsible for Deafness, Ectodermal Dysplasia, Craniosynostosis, Ectrodactyly, and Skeletal Anomaly Spectrum. [PDF]
Taşdelen E +5 more
europepmc +1 more source
Report of a novel UBA2 variant causing Aplasia Cutis Congenita with Ectrodactyly syndrome (ACCES) in an Indian family. [PDF]
Shirodkar AN +5 more
europepmc +1 more source
Ectrodactyly Ectodermal Dysplasia Cleft Lip (EEC) Syndrome. [PDF]
Kothari R, Kishore K, Chand S.
europepmc +1 more source
Identification of novel tumor protein 63 variant associated with split-hand/foot malformation and tooth agenesis. [PDF]
Long JY +6 more
europepmc +1 more source
A rare variant of oromandibular limb hypogenesis syndrome: a case report of glossopalatal ankylosis. [PDF]
Chopra S +4 more
europepmc +1 more source
Multidisciplinary management of nasal and lacrimal drainage disorders in ectrodactyly-ectodermal dysplasia-clefting syndrome. [PDF]
Bothra N, Lin LY, Bleier BS, Freitag SK.
europepmc +1 more source

