Fine-grained facial phenotype–genotype analysis in Wolf–Hirschhorn syndrome

Author:

Hammond Peter,Hannes Femke,Suttie Michael,Devriendt Koen,Vermeesch Joris Robert,Faravelli Francesca,Forzano Francesca,Parekh Susan,Williams Steve,McMullan Dominic,South Sarah T,Carey John C,Quarrell Oliver

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Reference41 articles.

1. Cooper H, Hirschhorn K : Apparent deletion of short arms of one chromosome (4 or 5) in a child with defects of midline fusion. Mamm Chrom Nwsl 1961; 4: 14.

2. Wolf U, Reinwein H, Porsch R, Schröter R, Baitsch H : Deficiency on the short arms of a chromosome no. 4. Humangenetik 1965; 1: 397–413.

3. Hirschhorn K, Cooper HL, Firschein IL : Deletion of short arms of chromosome 4–5 in a child with defects of midline fusion. Humangenetik 1965; 1: 479–482.

4. Battaglia A, Carey JC, South ST, Wright TJ : Wolf-Hirschhorn Syndrome; in: Pagon RA, Bird TD, Dolan CR, Stephens K, (eds). GeneReviews 2010 [Internet]. Seattle, WA: University of Washington, 1993–2002 (updated 17 June 2010).

5. Lurie IW, Lazjuk GI, Ussova YI, Presman EB, Gurevich DB : The Wolf–Hirschhorn syndrome. I. Genetics. Clin Genet 1980; 17: 375–384.

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