Results 131 to 140 of about 2,276 (204)

Morphological anomalies in amphibians of the Sierra Madre Occidental and a review of cases reported in Mexico. [PDF]

Environ Monit Assess
Castro-Bastidas HA, Bucio-Pacheco M, Serrano JM, Aguillón-Gutiérrez DR.   +3 more
europepmc   +1 more source

The Gollop-Wolfgang Complex: A Case Report. [PDF]

Pediatr Rep
Kim JB, Lee BR, Park JS, Hong CH, Kwon SW, Kim WJ, Wang SD, Lee DW, Nam KM, Jung KJ.   +9 more
europepmc   +1 more source

Ectrodactyly-polydactyly syndrome [PDF]

, 2020
openaire   +1 more source

CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy. [PDF]

Cureus
Danish E, Alsulami R, Baeshen H.
europepmc   +1 more source

Malformation Pattern and Molecular Findings in the <i>FGFR1</i>-Related Hartsfield Syndrome Phenotype. [PDF]

Med Sci (Basel)
Gaudioso F, Pascolini G.
europepmc   +1 more source

p63 in skin homeostasis and disease: molecular mechanisms and therapeutic potentials. [PDF]

Cell Death Discov
Cong Y, He Z, Hao H, Chen H, Chen A, Li C, Hu Y, Cong X.   +7 more
europepmc   +1 more source

Body stalk anomalies and their relationship to amniotic band disruption complex in six cats. [PDF]

J Feline Med Surg
Martín-Alguacil N, Cozar JM, Avedillo L.   +2 more
europepmc   +1 more source

Prenatal Ultrasound Evaluation of Congenital Hand Anomalies: Toward a Standardized Approach. [PDF]

J Med Ultrasound
Simeonova-Brachot II.
europepmc   +1 more source

Case Report: A new <i>UBA2</i> variant in a Chinese family with aplasia cutis congenita. [PDF]

Front Med (Lausanne)
He Y, Zhu S, Wei Q, Ye F, Ouyang X, Wu L, Li C.   +6 more
europepmc   +1 more source

Midline defect with corpus callosum agenesis, vermian hypoplasia and median cleft lip palate. [PDF]

Case Rep Perinat Med
Illi C, Koenigbauer JT, Weichert A.
europepmc   +1 more source