Report of a novel UBA2 variant causing Aplasia Cutis Congenita with Ectrodactyly syndrome (ACCES) in an Indian family. [PDF]
Clin DysmorpholShirodkar AN +5 more
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A rare variant of oromandibular limb hypogenesis syndrome: a case report of glossopalatal ankylosis. [PDF]
Front Dent MedChopra S +4 more
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Multidisciplinary management of nasal and lacrimal drainage disorders in ectrodactyly-ectodermal dysplasia-clefting syndrome. [PDF]
Saudi J OphthalmolBothra N, Lin LY, Bleier BS, Freitag SK.
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Morphological anomalies in amphibians of the Sierra Madre Occidental and a review of cases reported in Mexico. [PDF]
Environ Monit AssessCastro-Bastidas HA +3 more
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Malformation Pattern and Molecular Findings in the <i>FGFR1</i>-Related Hartsfield Syndrome Phenotype. [PDF]
Med Sci (Basel)Gaudioso F, Pascolini G.
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CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy. [PDF]
CureusDanish E, Alsulami R, Baeshen H.
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Body stalk anomalies and their relationship to amniotic band disruption complex in six cats. [PDF]
J Feline Med SurgMartín-Alguacil N +2 more
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p63 in skin homeostasis and disease: molecular mechanisms and therapeutic potentials. [PDF]
Cell Death DiscovCong Y +7 more
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Prenatal Ultrasound Evaluation of Congenital Hand Anomalies: Toward a Standardized Approach. [PDF]
J Med UltrasoundSimeonova-Brachot II.
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