F, Härle, C, Lengsfeld, H, Vahlenkamp
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Congenital Hypoglossia With Craniofacial Anomalies Without Limb Defects: A Rare Phenotypic Variant of Oromandibular-Limb Hypogenesis Syndrome. [PDF]
Ahiakpa AK +4 more
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Septic Arthritis: A Very Uncommon but Remarkable Complication Revealing Bertolotti Syndrome in a Child. [PDF]
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Advances in Functional Genomics for Human Health. [PDF]
Gonzales PR.
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Diagnosis of rare diseases based on facial phenotype: a quantitative assessment using 2D and 3D photography in Stickler syndrome. [PDF]
Rohée-Traoré A +8 more
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Very rare combination of Pierre Robin sequence with patent ductus arteriosus, severe persistent pulmonary hypertension, and sepsis in an Afghan neonate: a case report and literature review. [PDF]
Aslamzai M +3 more
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Systematic Management of a Critical CYP3A4 Interaction Between Cabozantinib and Carbamazepine: A Case Report of a Clinically Relevant Pharmacokinetic Interaction. [PDF]
Nizet P +4 more
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Next-Generation Sequencing Data and Clinical Features in Patients with Cleft Palate and Tooth Agenesis: A Systematic Literature Review. [PDF]
Boutahari N, Belayachi L, Ghoul S.
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