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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 26
2021 12
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548 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. Description of a Spanish cohort of 51 cases and a literature review].
Blanco-Lago R, Malaga-Dieguez I, Granizo-Martinez JJ, Carrera-Garcia L, Barruz-Galian P, Lapunzina P, Nevado-Blanco J, En Representacion Del Grupo Colaborativo Para El Estudio Del Sindrome de Wolf-Hirschhorn ERDGCPEEDSW. Blanco-Lago R, et al. Rev Neurol. 2017 May 1;64(9):393-400. Rev Neurol. 2017. PMID: 28444681 Free article. Review. Spanish.
INTRODUCTION: Wolf-Hirschhorn syndrome (WHS) is a contiguous gene syndrome that gives rise to multiple congenital anomalies, caused by the loss of a distal portion of the short arm of chromosome 4 (4p16.3). ...AIMS: To establish a register of patients …
INTRODUCTION: Wolf-Hirschhorn syndrome (WHS) is a contiguous gene syndrome that gives rise to multiple congenita …
[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 (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 …
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, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Mirzaa G, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2021. GeneReviews®. 1993–2021. 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 …
Natural histories of patients with Wolf-Hirschhorn syndrome derived from variable chromosomal abnormalities.
Yamamoto-Shimojima K, Kouwaki M, Kawashima Y, Itomi K, Momosaki K, Ozasa S, Okamoto N, Yokochi K, Yamamoto T. Yamamoto-Shimojima K, et al. Congenit Anom (Kyoto). 2019 Sep;59(5):169-173. doi: 10.1111/cga.12318. Epub 2018 Nov 15. Congenit Anom (Kyoto). 2019. PMID: 30378700
Wolf-Hirschhorn syndrome (WHS) is a subtelomeric deletion syndrome affecting the short arm of chromosome 4. ...
Wolf-Hirschhorn syndrome (WHS) is a subtelomeric deletion syndrome affecting the short arm of chromosome 4. ...
International meeting on Wolf-Hirschhorn syndrome: Update on the nosology and new insights on the pathogenic mechanisms for seizures and growth delay.
Nevado J, Ho KS, Zollino M, Blanco R, Cobaleda C, Golzio C, Beaudry-Bellefeuille I, Berrocoso S, Limeres J, Barrúz P, Serrano-Martín C, Cafiero C, Málaga I, Marangi G, Campos-Sánchez E, Moriyón-Iglesias T, Márquez S, Markham L, Twede H, Lortz A, Olson L, Sheng X, Weng C, Wassman ER 3rd, Newcomb T, Wassman ER, Carey JC, Battaglia A, López-Granados E; Wolf-Hirschhorn Spain's Working Group, Douglas D, Lapunzina P. Nevado J, et al. Am J Med Genet A. 2020 Jan;182(1):257-267. doi: 10.1002/ajmg.a.61406. Epub 2019 Nov 25. Am J Med Genet A. 2020. PMID: 31769173
"An International Meeting on Wolf-Hirschhorn Syndrome (WHS)" was held at The University Hospital La Paz in Madrid, Spain (October 13-14, 2017). ...
"An International Meeting on Wolf-Hirschhorn Syndrome (WHS)" was held at The University Hospital La Paz in Madrid, Spai …
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 …
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