Wolf-Hirschhorn (4p-) syndrome in adults

Genetic Counseling

Volumn 12, Issue 1, 2001, Pages 35-48

  Marcelis, C ^a   Schrander Stumpel, C ^a   Engelen, J ^a   Schoonbrood Lenssen, A ^a   Willemse, A ^a   Beemer, F ^a   Sigaudy, S ^a   Missirian, C ^a   Philip, N ^a   Fryns, J P ^a  

^a MAASTRICHT UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

4p deletion; Adult phenotype; Pitt Rogers Danks Syndrome; Wolf Hirschhorn syndrome

Indexed keywords

ADULT; ARTICLE; CASE REPORT; CHROMOSOME 4P; CHROMOSOME DELETION 4; CLINICAL EXAMINATION; DISEASE SEVERITY; FAMILY COUNSELING; FEMALE; HUMAN; MALE; PATIENT COUNSELING; PHENOTYPE; SYNDROME DELINEATION; WOLF HIRSCHHORN SYNDROME;

ABNORMALITIES, MULTIPLE; ADULT; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 4; FEMALE; HUMANS; MALE; MENTAL RETARDATION; SYNDROME;

CANIS;

EID: 0035086406     PISSN: 10158146     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (35)

1. Molecular confirmation of Wolf-Hirschhorn syndrome with a subtle translocation of chromosome 4
2. Molecular detection of a 4p deletion using PCR-based polymorphisms: A technique for the rapid detection of the Wolf-Hirschhorn syndrome
3. Wolf-Hirschhorn syndrome and Pitt-Rogers-Danks syndrome
4. Natural history of Wolf-Hirschhorn syndrome: Experience with 15 cases
5. Wolf-Hirschhorn syndrome (WHS): A history in pictures
6. Pitt-Rogers-Danks Syndrome: The result of a 4p microdeletion
7. 11q duplication in a patient with Pitt-Rogers-Danks phenotype
8. Editorial comment: Pitt-Rogers-Danks syndrome and Wolf-Hirschhorn syndrome
9. Summary of the 1993 ASHG ancillary meeting «Recent research on chromosome 4p syndromes and genes»
10. The 4p- syndrome in a 24-year-old female
11. Growth retardation in Wolf-Hirschhorn syndrome
12. A family with three sisters with the 4p- syndrome, originally reported as suffering from the Smith-Lemli-Opitz syndrome
13. Deletion of short arms of chromosome 4-5 in a child with defects of midline fusion
14. The Wolf-Hirschhorn (4p-) syndrome
15. Pitt-Rogers-Danks syndrome and Wolf-Hirschhorn syndrome are caused by a deletion in the same region on chromosome 4p16.3
16. Cytogenetic abnormalities in two new patients with Pitt-Rogers-Danks phenotype
17. The Wolf-Hirschhorn syndrome. I
18. Deletion of chromosome 4p detected by FISH in a girl with normal high-resolution karyotype
19. The Wolf-Hirschhorn syndrome in adulthood: Evaluation of a 24-year-old man with a rec(4) chromosome
20. Twenty-seven-year follow up in the Wolf-Hirschhorn Syndrome
21. Translocations involving 4p16.3 in three families: Deletion causing the Pitt-Rogers-Danks syndrome and duplication resulting in a new overgrowth syndrome
22. Wolf-Hirschhorn and Pitt-Rogers-Danks Syndromes
23. Mental retardation, unusual face, and intrauterine growth retardation
24. A taxonomic approach to the del(4p) phenotype
25. Familial Wolf-Hirschhorn syndrome resulting from a cryptic translocation: A clinical and molecular study
26. Long-term survival in the Wolf-Hirschhorn (4p-) syndrome
27. WHSC1, a 90 kb SET domain-containing gene, expressed in early development and homologous to a drosophila dysmorphy gene maps in the Wolf-Hirschhorn-syndrome critical region and is fused to lgH in t(4;14) multiple myeloma
28. Familial translocation resulting in Wolf-Hirschhorn Syndrome in two related unbalanced individuals: Clinical evaluation of a 39-year-old man with Wolf-Hirschhorn syndrome
29. Genetic and clinical study in 13 patients with the Wolf-Hirschhorn syndrome [del(4p)]
30. Defizienz an den kurzen armen eines chromosoms nr. 4
31. Wolf-Hirschhorn and Pitt-Rogers-Danks Syndromes caused by overlapping 4p deletions
32. A transcript map of the newly defined 165 kb Wolf-Hirschhorn syndrome critical region
33. Reply to the letter to the editor by Partington and Turner - «Wolf-Hirschhorn and Pitt-Rogers-Danks syndromes»
34. From Pitt-Rogers-Danks syndrome to Wolf-Hirschhorn syndrome and back?