PubMed (OMIM) for id: 408255

Year	Number of Results
1985	1
1987	1
1991	3
1992	5
1997	1
1998	1
1999	1
2000	3
2001	3
2002	1
2003	2
2004	1
2024	0

1

Mild Wolf-Hirschhorn syndrome: micro-array CGH analysis of atypical 4p16.3 deletions enables refinement of the genotype-phenotype map.

Van Buggenhout G, Melotte C, Dutta B, Froyen G, Van Hummelen P, Marynen P, Matthijs G, de Ravel T, Devriendt K, Fryns JP, Vermeesch JR. Van Buggenhout G, et al. J Med Genet. 2004 Sep;41(9):691-8. doi: 10.1136/jmg.2003.016865. J Med Genet. 2004. PMID: 15342700 Free PMC article. No abstract available.

2

MSX1 gene is deleted in Wolf-Hirschhorn syndrome patients with oligodontia.

Nieminen P, Kotilainen J, Aalto Y, Knuutila S, Pirinen S, Thesleff I. Nieminen P, et al. J Dent Res. 2003 Dec;82(12):1013-7. doi: 10.1177/154405910308201215. J Dent Res. 2003. PMID: 14630905

3

Mapping the Wolf-Hirschhorn syndrome phenotype outside the currently accepted WHS critical region and defining a new critical region, WHSCR-2.

Zollino M, Lecce R, Fischetto R, Murdolo M, Faravelli F, Selicorni A, Buttè C, Memo L, Capovilla G, Neri G. Zollino M, et al. Am J Hum Genet. 2003 Mar;72(3):590-7. doi: 10.1086/367925. Epub 2003 Jan 30. Am J Hum Genet. 2003. PMID: 12563561 Free PMC article.

4

Heterozygous submicroscopic inversions involving olfactory receptor-gene clusters mediate the recurrent t(4;8)(p16;p23) translocation.

Giglio S, Calvari V, Gregato G, Gimelli G, Camanini S, Giorda R, Ragusa A, Guerneri S, Selicorni A, Stumm M, Tonnies H, Ventura M, Zollino M, Neri G, Barber J, Wieczorek D, Rocchi M, Zuffardi O. Giglio S, et al. Am J Hum Genet. 2002 Aug;71(2):276-85. doi: 10.1086/341610. Epub 2002 Jun 10. Am J Hum Genet. 2002. PMID: 12058347 Free PMC article.

5

An epidemiological study of Wolf-Hirschhorn syndrome: life expectancy and cause of mortality.

Shannon NL, Maltby EL, Rigby AS, Quarrell OW. Shannon NL, et al. J Med Genet. 2001 Oct;38(10):674-9. doi: 10.1136/jmg.38.10.674. J Med Genet. 2001. PMID: 11584045 Free PMC article.

6

Olfactory receptor-gene clusters, genomic-inversion polymorphisms, and common chromosome rearrangements.

Giglio S, Broman KW, Matsumoto N, Calvari V, Gimelli G, Neumann T, Ohashi H, Voullaire L, Larizza D, Giorda R, Weber JL, Ledbetter DH, Zuffardi O. Giglio S, et al. Am J Hum Genet. 2001 Apr;68(4):874-83. doi: 10.1086/319506. Epub 2001 Feb 26. Am J Hum Genet. 2001. PMID: 11231899 Free PMC article.

7

Unexpected high frequency of de novo unbalanced translocations in patients with Wolf-Hirschhorn syndrome (WHS).

Wieczorek D, Krause M, Majewski F, Albrecht B, Meinecke P, Riess O, Gillessen-Kaesbach G. Wieczorek D, et al. J Med Genet. 2000 Oct;37(10):798-804. doi: 10.1136/jmg.37.10.798. J Med Genet. 2000. PMID: 11183188 Free PMC article. No abstract available.

8

Mouse models for the Wolf-Hirschhorn deletion syndrome.

Näf D, Wilson LA, Bergstrom RA, Smith RS, Goodwin NC, Verkerk A, van Ommen GJ, Ackerman SL, Frankel WN, Schimenti JC. Näf D, et al. Hum Mol Genet. 2001 Jan 15;10(2):91-8. doi: 10.1093/hmg/10.2.91. Hum Mol Genet. 2001. PMID: 11152656

9

Alu-mediated PCR artifacts and the constitutional t(11;22) breakpoint.

Kurahashi H, Shaikh TH, Emanuel BS. Kurahashi H, et al. Hum Mol Genet. 2000 Nov 1;9(18):2727-32. doi: 10.1093/hmg/9.18.2727. Hum Mol Genet. 2000. PMID: 11063731

10

Genotype-phenotype correlations and clinical diagnostic criteria in Wolf-Hirschhorn syndrome.

Zollino M, Di Stefano C, Zampino G, Mastroiacovo P, Wright TJ, Sorge G, Selicorni A, Tenconi R, Zappalà A, Battaglia A, Di Rocco M, Palka G, Pallotta R, Altherr MR, Neri G. Zollino M, et al. Am J Med Genet. 2000 Sep 18;94(3):254-61. doi: 10.1002/1096-8628(20000918)94:3<254::aid-ajmg13>3.0.co;2-7. Am J Med Genet. 2000. PMID: 10995514

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