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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1970 1
1971 2
1975 2
1976 1
1977 2
1978 1
1979 3
1980 4
1981 3
1982 1
1983 1
1984 2
1985 6
1986 4
1987 4
1988 2
1989 3
1990 6
1991 6
1992 12
1993 7
1994 10
1995 12
1996 12
1997 6
1998 16
1999 12
2000 16
2001 18
2002 10
2003 10
2004 19
2005 15
2006 9
2007 19
2008 29
2009 20
2010 26
2011 18
2012 20
2013 30
2014 27
2015 21
2016 23
2017 30
2018 26
2019 25
2020 28
2021 25
2022 19
2023 1
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577 results
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Page 1
Wolf-Hirschhorn syndrome: A review and update.
Battaglia A, Carey JC, South ST. Battaglia A, et al. Am J Med Genet C Semin Med Genet. 2015 Sep;169(3):216-23. doi: 10.1002/ajmg.c.31449. Epub 2015 Aug 4. Am J Med Genet C Semin Med Genet. 2015. PMID: 26239400 Review.
Wolf-Hirschhorn syndrome (WHS) - literature review on the features of the syndrome.
Paradowska-Stolarz AM. Paradowska-Stolarz AM. Adv Clin Exp Med. 2014 May-Jun;23(3):485-9. doi: 10.17219/acem/24111. Adv Clin Exp Med. 2014. PMID: 24979523 Free article. Review.
Wolf-Hirschhorn syndrome (WHS) is a congenital disorder associated with 4 chromosome microdeletion. ...The characteristic thing is that the more genetic material is missing, the more pronounced are the dimorphic features of the syndrome. Mostly, the de …
Wolf-Hirschhorn syndrome (WHS) is a congenital disorder associated with 4 chromosome microdeletion. ...The characterist …
Clinical and epilepsy characteristics in Wolf-Hirschhorn syndrome (4p-): A review.
Paprocka J, Kaminiów K, Yetkin O, Tekturk P, Baykan B, Leiz S, Kluger G, Striano P. Paprocka J, et al. Seizure. 2022 Dec 8:S1059-1311(22)00277-1. doi: 10.1016/j.seizure.2022.12.001. Online ahead of print. Seizure. 2022. PMID: 36526544 Review.
Wolf-Hirschhorn syndrome (WHS) is araredisorderwithan estimated prevalence being around 1 in 50,000 births. The syndrome is caused by the deletion of a critical region (Wolf-Hirschhorn Syndrome Critical region- WHSCR) on chromosome …
Wolf-Hirschhorn syndrome (WHS) is araredisorderwithan estimated prevalence being around 1 in 50,000 births. The synd …
Wolf-Hirschhorn (4p-) syndrome.
Battaglia A, Carey JC, Wright TJ. Battaglia A, et al. Adv Pediatr. 2001;48:75-113. Adv Pediatr. 2001. PMID: 11480768 Review.
Wolf-Hirschhorn syndrome (WHS) is a well-known congenital malformation syndrome caused by deletion of the short arm of chromosome 4 (4p-). ...Although thought to affect 1 per 50,000 births, we believe that the syndrome is more common because of …
Wolf-Hirschhorn syndrome (WHS) is a well-known congenital malformation syndrome caused by deletion of the short …
The delineation of the Wolf-Hirschhorn syndrome over six decades: Illustration of the ongoing advances in phenotype analysis and cytogenomic technology.
Battaglia A, Carey JC. Battaglia A, et al. Am J Med Genet A. 2021 Sep;185(9):2748-2755. doi: 10.1002/ajmg.a.62341. Epub 2021 May 18. Am J Med Genet A. 2021. PMID: 34002939 Review.
Since Hirschhorn's description in 1961, the history and chronology of the clinical, cytogenetic, and molecular characterization of Wolf-Hirschhorn syndrome (WHS) elegantly demonstrates the remarkable advances in genetic technology over the last six dec …
Since Hirschhorn's description in 1961, the history and chronology of the clinical, cytogenetic, and molecular characterization of …
A practical approach to dental care for patients with Wolf-Hirschhorn syndrome.
Serrano Martín C, Fernández Feijoo J, García Mato E, Varela Aneiros I, Diniz Freitas M, Vázquez García E, Limeres Posse J. Serrano Martín C, et al. Spec Care Dentist. 2022 Mar;42(2):137-142. doi: 10.1111/scd.12644. Epub 2021 Sep 19. Spec Care Dentist. 2022. PMID: 34538003 Review.
Wolf-Hirschhorn syndrome is a polymalformative chromosomal disorder caused by a deletion in the distal region of the short arm of chromosome 4. ...The most prevalent oral manifestations are hypodontia, delayed tooth eruption, morphological dental abnormalitie …
Wolf-Hirschhorn syndrome is a polymalformative chromosomal disorder caused by a deletion in the distal region of the sh …
Wolf-Hirschhorn Syndrome – RETIRED CHAPTER, FOR HISTORICAL REFERENCE ONLY.
Battaglia A, Carey JC, South ST. Battaglia A, et al. 2002 Apr 29 [updated 2015 Aug 20]. In: Adam MP, Everman DB, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2023. 2002 Apr 29 [updated 2015 Aug 20]. In: Adam MP, Everman DB, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2023. PMID: 20301362 Free Books & Documents. Review.
THIS ARCHIVAL VERSION IS FOR HISTORICAL REFERENCE ONLY, AND THE INFORMATION MAY BE OUT OF DATE. CLINICAL CHARACTERISTICS: Wolf-Hirschhorn syndrome (WHS) is characterized by typical craniofacial features in infancy consisting of "Greek warrior helmet" appearan …
THIS ARCHIVAL VERSION IS FOR HISTORICAL REFERENCE ONLY, AND THE INFORMATION MAY BE OUT OF DATE. CLINICAL CHARACTERISTICS: Wolf-Hir …
From Wolf-Hirschhorn syndrome to NSD2 haploinsufficiency: a shifting paradigm through the description of a new case and a review of the literature.
Wiel LC, Bruno I, Barbi E, Sirchia F. Wiel LC, et al. Ital J Pediatr. 2022 May 12;48(1):72. doi: 10.1186/s13052-022-01267-w. Ital J Pediatr. 2022. PMID: 35550183 Free PMC article. Review.
BACKGROUND: Wolf-Hirschhorn syndrome (WHS) is a well-defined disorder, whose core phenotype encompasses growth restriction, facial gestalt, intellectual disability and seizures. ...CONCLUSIONS: Full WHS phenotype likely arises from the cumulative effect of th …
BACKGROUND: Wolf-Hirschhorn syndrome (WHS) is a well-defined disorder, whose core phenotype encompasses growth restrict …
[The Wolf-Hirschhorn Syndrome].
Friebe-Hoffmann U, Reister F, Gaspar H, Hummler H, Lindner W, Lato K. Friebe-Hoffmann U, et al. Z Geburtshilfe Neonatol. 2016 Oct;220(5):195-199. doi: 10.1055/s-0042-107084. Epub 2016 May 20. Z Geburtshilfe Neonatol. 2016. PMID: 27203859 Review. German.
Wolf-Hirschhorn syndrome (WHS) represents a complex developmental disorder characterized by craniofacial dysmorphism, short stature, hypotonia, psychomotor retardation and seizures caused by a terminal deletion of the short arm of chromosome 4. ...
Wolf-Hirschhorn syndrome (WHS) represents a complex developmental disorder characterized by craniofacial dysmorphism, s …
Wolf-Hirschhorn syndrome.
Coffin GS, Wilson MG. Coffin GS, et al. Am J Dis Child. 1971 Mar;121(3):265. doi: 10.1001/archpedi.1971.02100140131020. Am J Dis Child. 1971. PMID: 5575893 No abstract available.
577 results

Searches related to "wolf hirschhorn syndrome"