The evolving craniofacial phenotype of a patient with Sensenbrenner syndrome caused by IFT140 compound heterozygous mutations-MedSci.cn - 梅斯（MedSci）

The evolving craniofacial phenotype of a patient with Sensenbrenner syndrome caused by IFT140 compound heterozygous mutations

Bayat, A; Kerr, B; Douzgou, S

Douzgou, S (reprint author), Univ Manchester, Cent Manchester Univ Hosp NHS Fdn Trust, Manchester Ctr Genom Med,Sch Biol Sci, St Marys Hosp,Manchester Acad Hlth Sci Ctr,Div Ev, Oxford Rd, Manchester M13 9WL, Lancs, England.

CLINICAL DYSMORPHOLOGY, 2017; 26 (4): 247

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