Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Filters
Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2002 | 1 |
2004 | 1 |
2012 | 1 |
2014 | 1 |
2024 | 0 |
Search Results
4 results
Results by year
Filters applied: . Clear all
Quoted phrase not found in phrase index: "Syndrome with limb duplication, polydactyly, syndactyly, and/or hyperphalangy"
Page 1
Congenital malformations of the hand and forearm in children: what radiologists should know.
Semin Musculoskelet Radiol. 2012 Apr;16(2):146-58. doi: 10.1055/s-0032-1311766. Epub 2012 May 30.
Semin Musculoskelet Radiol. 2012.
PMID: 22648430
Review.
They can be divided into (1) failure of formation with transverse, intercalary, and longitudinal (preaxial, postaxial, and mesoaxial) deficiencies, (2) failure of differentiation with synostoses, carpal coalitions, syndactylies, and symphalangism, (3) duplication wi …
They can be divided into (1) failure of formation with transverse, intercalary, and longitudinal (preaxial, postaxial, and mesoaxial) defici …
Homozygous and compound-heterozygous mutations in TGDS cause Catel-Manzke syndrome.
Ehmke N, Caliebe A, Koenig R, Kant SG, Stark Z, Cormier-Daire V, Wieczorek D, Gillessen-Kaesbach G, Hoff K, Kawalia A, Thiele H, Altmüller J, Fischer-Zirnsak B, Knaus A, Zhu N, Heinrich V, Huber C, Harabula I, Spielmann M, Horn D, Kornak U, Hecht J, Krawitz PM, Nürnberg P, Siebert R, Manzke H, Mundlos S.
Ehmke N, et al.
Am J Hum Genet. 2014 Dec 4;95(6):763-70. doi: 10.1016/j.ajhg.2014.11.004.
Am J Hum Genet. 2014.
PMID: 25480037
Free PMC article.
Catel-Manzke syndrome is characterized by Pierre Robin sequence and a unique form of bilateral hyperphalangy causing a clinodactyly of the index finger. We describe the identification of homozygous and compound heterozygous mutations in TGDS in seven unrelated individuals …
Catel-Manzke syndrome is characterized by Pierre Robin sequence and a unique form of bilateral hyperphalangy causing a clinodactyly o …
Item in Clipboard
Van der Woude syndrome with sensorineural hearing loss, large craniofacial sinuses, dental pulp stones, and minor limb anomalies: report of a four-generation Thai family.
Kantaputra PN, Sumitsawan Y, Schutte BC, Tochareontanaphol C.
Kantaputra PN, et al.
Am J Med Genet. 2002 Apr 1;108(4):275-80. doi: 10.1002/ajmg.10276.
Am J Med Genet. 2002.
PMID: 11920830
A four-generation Thai family affected with Van der Woude syndrome is reported. The disorder appeared to be originally inherited from a person who was half Thai and half Pakistani. ...
A four-generation Thai family affected with Van der Woude syndrome is reported. The disorder appeared to be originally inherited from …
Item in Clipboard
Simplicity and treatment of the typical cleft hand.
Upton J.
Upton J.
Handchir Mikrochir Plast Chir. 2004 Apr-Jun;36(2-3):152-60. doi: 10.1055/s-2004-817903.
Handchir Mikrochir Plast Chir. 2004.
PMID: 15162314
These difficult surgical corrections may often include index transposition, metacarpal and/or phalangeal osteotomies, joint releases, phalangeal ostectomies, preservation of the adductor pollicis muscle, first dorsal interosseous muscle release, syndactyly separation(s) an …
These difficult surgical corrections may often include index transposition, metacarpal and/or phalangeal osteotomies, joint releases, phalan …
Item in Clipboard
Cite
Cite