Wolf-Hirschhorn syndrome (WHS): A history in pictures

Clinical Dysmorphology

Volumn 9, Issue 1, 2000, Pages 25-30

  Battaglia, Agatino ^a,b   Carey, J C ^b   Viskochil, D H ^b   Cederholm, P ^b   Opitz, J M ^b  

^a DEPARTMENT OF DEVELOPMENTAL NEUROSCIENCE   (Italy)

^b UNIVERSITY OF UTAH SCHOOL OF MEDICINE   (United States)

Author keywords

Change with age; Clinical phenotype; Deletion 4p syndrome; Wolf Hirschhorn syndrome

Indexed keywords

ARTICLE; CHROMOSOME DELETION 4; FACE MALFORMATION; HUMAN; PHENOTYPE; PRIORITY JOURNAL; WOLF HIRSCHHORN SYNDROME;

EID: 0033954143     PISSN: 09628827     EISSN: None     Source Type: Journal    
DOI: 10.1097/00019605-200009010-00005     Document Type: Article

References (9)

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2. Battaglia A, Carey JC, Cederholm P, Viskochil D, Brothman AR, Galasso C (1999). Natural history of Wolf-Hirschhorn syndrome: experience with 15 cases. Pediatrics 103: 830-836.
3. Bull MJ, Warburton D (1990). Chromosome 4, monosomy 4p. In: Buyse ML, (editor) Birth Defects Encyclopedia. Cambridge, MA: Blackwell Scientific Publications pp. 334-335.
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5. Hirschhorn K, Cooper H, Firschein IL (1965). Deletion of short arms of chromosome 4-5 in a child with defects of midline fusion. Humangenetik 1:479-482.
6. Jones KL (1997). Smith's Recognizable patterns of human malformation, 5th edition. Philadelphia: W. B. Saunders Company pp. 38-39.
7. Opitz MJ (1995). Twenty-seven-year follow-up in the Wolf-Hirschhorn syndrome. Am J Med Genet 55: 459-461.
8. Wheeler PG, Weaver DD, Palmer CG (1995). Familial translocation resulting in Wolf-Hirschhorn syndrome in two related unbalanced individuals: clinical evaluation of a 39-year-old man with Wolf-Hirschhorn syndrome. Am J Med Genet 55:462-465.
9. Wolf U, Reinwein H, Porsh R, Schroter R, Baitsch (1965). Defizienz am den kurze Armen eines chromosomes nr. 4. Humangenetik 1:397-413.