Absent mandibular gap in the retronasal triangle view: a clue to the diagnosis of micrognathia in the first trimester. (33/70)

Finding disease variants in Mendelian disorders by using sequence data: methods and applications. (34/70)

Mandibular distraction in neonates: indications, technique, results. (35/70)

Hereditary sclerosing poikiloderma. (36/70)

Meier-Gorlin syndrome genotype-phenotype studies: 35 individuals with pre-replication complex gene mutations and 10 without molecular diagnosis. (37/70)

The BAH domain of ORC1 links H4K20me2 to DNA replication licensing and Meier-Gorlin syndrome. (38/70)

Informed consent for whole genome sequencing: a qualitative analysis of participant expectations and perceptions of risks, benefits, and harms. (39/70)

Miller (Genee-Wiedemann) syndrome represents a clinically and biochemically distinct subgroup of postaxial acrofacial dysostosis associated with partial deficiency of DHODH. (40/70)

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