Wolf-Hirschhorn syndrome and Pitt-Rogers
โ Battaglia, Agatino; Carey, John C.
๐ Article
๐
1998
๐ John Wiley and Sons
๐ English
โ 2 KB
๐ 1 views
โฆ LIBER โฆ
Wolf-Hirschhorn and Pitt-Rogers-Danks syndromes
โ Scribed by Partington, Michael; Turner, Gillian
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 1 KB
- Volume
- 82
- Category
- Article
- ISSN
- 0148-7299
- DOI
- 10.1002/(sici)1096-8628(19990101)82:1<88::aid-ajmg17>3.0.co;2-0
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Wolf-Hirschhorn and Pitt-Rogers-Danks sy
โ Wright, Tracy J.; Clemens, Michele; Quarrell, Oliver; Altherr, Michael R.
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Wolf-Hirschhorn syndrome (WHS), a multiple congenital malformation syndrome, and Pitt-Rogers-Danks syndrome (PRDS), a rare condition with similar anomalies, were previously thought to be clinically distinct conditions. While WHS has long been associated with deletions near the terminus of 4p, severa
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๐ 2 views
Ectrodactyly has not previously been reported in children with Wolf-Hirschhorn syndrome (WHS). Based on this premise and the identification of an unbalanced translocation between chromosomes 4p15 and 10q25 in a fetus with ectrodactyly and hemimelia, a second locus for dominantly inherited split hand
Reply to the letter to the editor by Par
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๐ John Wiley and Sons
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Health supervision and anticipatory guid
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Wolf-Hirschhorn syndrome (WHS) is a well-known malformation syndrome due to microdeletion of the short arm of chromosome 4 (4pโซ.)ืโฌ Almost 120 cases have been reported so far, yet there is still limited information on its natural history. It is generally thought that these children have severe devel
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Wolf-Hirschhorn syndrome (WHS) is a multiple anomaly condition characterized by mental and developmental defects, resulting from the absence of the distal segment of one chromosome 4 short arm (4p16.3). Owing to the complex and variable expression of this disorder, it is thought that the WHS is a co