From Pitt-Rogers-Danks syndrome to Wolf-Hirschhorn syndrome. and back?

American Journal of Medical Genetics - Seminars in Medical Genetics

Volumn 66, Issue 1, 1996, Pages 113-115

  Zollino, Marcella ^a,b   Bova, Renato ^a   Neri, Giovanni ^a  

^a CATHOLIC UNIVERSITY   (Italy)

^b CATHOLIC UNIVERSITY   (Italy)

Author keywords

Aneuploidy syndrome; Fluorescent in situ hybridization; Pitt Rogers Danks syndrome; Wolf Hirschhorn syndrome

Indexed keywords

CANIS;

ARTICLE; CASE REPORT; CHILD; CHROMOSOME 4P; CHROMOSOME ANALYSIS; CHROMOSOME DELETION 4; DISEASE CLASSIFICATION; FLUORESCENCE IN SITU HYBRIDIZATION; GENE; HUMAN; MALE; PHENOTYPE; POINT MUTATION; PRIORITY JOURNAL; WOLF HIRSCHHORN SYNDROME;

ABNORMALITIES, MULTIPLE; CHROMOSOMES, HUMAN, PAIR 4; FACE; GENE DELETION; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; MALE; SYNDROME;

EID: 0029914013     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19961202)66:1<113::AID-AJMG29>3.0.CO;2-U     Document Type: Article

References (6)

1. Clemens M, Martsolf JT, Rogers JG, Mowery-Rushton P, Surti U, McPherson E (1996).Pitt-Rogers-Danks syndrome: The result of a 4p microdeletion. Am J Med Genet, this issue.
2. Donnai D (1996): Editorial comment. Pitt-Rogers-Danks syndrome and Wolf-Hirschhorn syndrome. Am J Med Genet, this issue.
3. Estabrooks LL, Rao WR, Driscoll DA, Crandall BF, Dean CS, Ikonen E, Korg B, Aylsworth S (1995): Preliminary phenotypic map of chromosome 4p16 based on 4p deletions. Am J Med Genet 57: 581-586.
4. Gandelman KY, Gibson L, Meyn MS, Yang-Feng L (1992): Molecular definition of the smallest region of deletion overlap in the Wolf-Hirschhorn syndrome. Am J Med Gene 51: 571-578.
5. Lindeman-Kusse MC, Van Haeringen A, Hoorweg JJG, Brunner HG (1996) : Cytogenetic abnormalities in two new patients with Pitt-Rogers-Danks phenotype. Am J Med Genet, this issue.
6. Wright TJ, Denison K, Altherr MR (1995): Redefinition and molecular analysis of the critical region for the Wolf-Hirschhorn syndrome locus. Am J Hum Genet 57 (suppl): A233.