A Rare Case of Concurrent SNRPB Mutation and 22q11.2 Microduplication in a Child With Cerebro-Costo-Mandibular Syndrome. [PDF]
Slear E, Thompson C, Ruas V.
europepmc +1 more source
Trisomy 9 mosaicism: a genetic disorder with complications-a case report. [PDF]
Ajour M +3 more
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The laryngeal mask airway in the extraction of supernumerary teeth in children: a retrospective study. [PDF]
Qi F +5 more
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Endocrine Phenotypes and Hormonal Treatment in Meier-Gorlin Syndrome: Report of Two Cases and a Systematic Review of Literature. [PDF]
Swapnil K +7 more
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A conceptual clinical reasoning framework for early syndromic recognition in dental practice. [PDF]
Shqaidef A +3 more
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A rare variant of oromandibular limb hypogenesis syndrome: a case report of glossopalatal ankylosis. [PDF]
Chopra S +4 more
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Hajdu-Cheney Syndrome as a Rare Cause of Acroosteolysis: A Case Report. [PDF]
Nahi C +5 more
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Prenatal Ultrasound Detection and Neonatal Nasogastric Tube Feeding Follow Opposite Gradients Across Orofacial Cleft Phenotypes: A Nationally Ascertained Referral-Centre Cohort Study. [PDF]
Tarle A +4 more
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Integrating imaging and genomics in prenatal Treacher Collins syndrome: evidence for practice and policy. [PDF]
Li C +7 more
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