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Clinical Phenotype of FOXP1 Syndrome: Parent-Reported Medical Signs and Symptoms in 40 Individuals.

Saskia Koene,Fabienne Gwendolin Ropers,Jannelien Wieland,Tamara Rybak,Floor Wildschut,Dagmar Berghuis,Angela Morgan,Maria Pilar Trelles,Jeroen Ronald Scheepe,Regina Boekenkamp,Cacha M. P. C. D. Peeters-Scholte,Ruth Braden,Gijs W. E. Santen

JOURNAL OF MEDICAL GENETICS（2024）

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关键词
Inborn Genetic Diseases,Genetic Counselling,Genetics, Medical,Patient Care,Phenotype
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