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Hand polydactyly
Known as:
Polydactyly of fingers
, Supernumerary finger
, Extra finger
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A kind of polydactyly characterized by the presence of a supernumerary finger or fingers. [HPO:probinson]
National Institutes of Health
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Related topics
Related topics
3 relations
Broader (1)
Polydactyly
Radial polydactyly
accessory organ
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2016
2016
Efficiency of Human Epiphyseal Chondrocytes with Differential Replication Numbers for Cellular Therapy Products
Michiyo Nasu
,
S. Takayama
,
A. Umezawa
BioMed Research International
2016
Corpus ID: 15894373
The cell-based therapy for cartilage or bone requires a large number of cells; serial passages of chondrocytes are, therefore…
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2015
2015
A single mass two-axis capacitive MEMS accelerometer with force rebalance
Talha Köse
,
Yunus Terzioglu
,
K. Azgın
,
T. Akin
Proceedings
2015
Corpus ID: 38999844
This paper presents a single mass 2-axis MEMS capacitive accelerometer with a unique force rebalance method achieved with the…
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2014
2014
Fabrication and Improved Performance of GaN LEDs With Finger-Type Structure
Ken-Yen Chen
,
Ching-Ho Tien
,
Chen‐Peng Hsu
,
Chao-Yu Pai
,
R. Horng
IEEE Transactions on Electron Devices
2014
Corpus ID: 46307127
This paper demonstrates that vertical gallium nitride (GaN) light-emitting diodes (LEDs) with a finger-type current spreading…
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2014
2014
A novel nonsense mutation in BBS4 gene identified in a Chinese family with Bardet‐Biedl syndrome
Qian Li
,
Yongpeng Zhang
,
Liyun Jia
,
Xiaoyan Peng
Chinese Medical Journal
2014
Corpus ID: 3244884
Background Bardet‐Biedl syndrome (BBS) is a genetically heterogeneous disease, and information about BBS in Chinese populations…
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2013
2013
Prenatal diagnosis of mosaic trisomy 2 associated with abnormal maternal serum screening, oligohydramnios, intrauterine growth restriction, ventricular septal defect, preaxial polydactyly, and facial…
Chih-ping Chen
,
Yi-Yung Chen
,
+6 authors
Wayseen Wang
Taiwanese Journal of Obstetrics & Gynecology
2013
Corpus ID: 205418230
2007
2007
Polymelia associated with frequent chromosome breaks in a heifer
J. Nowacka
,
K. Urbaniak
,
P. Antosik
,
J. Jaśkowski
,
H. Frąckowiak
,
M. Świtoński
The Veterinary Record
2007
Corpus ID: 44881171
POLYMELIA is a rare congenital defect characterised by the presence of a supernumerary limb at different locations on the body…
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2005
2005
Six cases of deletion 9p24 and trisomy 19q13.4 inherited from a familial balanced translocation.
P. Su
,
P. Kuo
,
Suh-Jen Chen
,
Shu-Chi Huang
,
Jia-yuh Chen
,
Huei-Mei Hung
Journal of the Formosan Medical Association…
2005
Corpus ID: 41188604
The deletion 9p with trisomy 19q syndrome is a rare disorder. We report 2 adults and 4 children with deletion 9p and trisomy 19q…
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2000
2000
Sibs with anencephaly, anophthalmia, clefts, omphalocele, and polydactyly: hydrolethalus or acrocallosal syndrome?
B. Christensen
,
H. Blaas
,
C. Isaksen
,
B. Roald
,
K. Orstavik
American journal of medical genetics
2000
Corpus ID: 35209667
Major characteristics of the acrocallosal syndrome include severe mental retardation, agenesis or hypoplasia of the corpus…
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Review
1997
Review
1997
Acrocallosal syndrome in an Algerian boy born to consanguineous parents: review of the literature and further delineation of the syndrome.
W. Courtens
,
E. Vamos
,
Catherine Christophe
,
A. Schinzel
American journal of medical genetics
1997
Corpus ID: 42380685
We present a 17-month-old boy with the acrocallosal syndrome. He was born to consanguineous parents. Abnormal findings included…
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1997
1997
Polydactyly of the foot: manifestations and treatment.
Hongsen Chiang
,
Shier-Chieg Huang
Journal of the Formosan Medical Association…
1997
Corpus ID: 24942171
Polydactyly of the foot is not an uncommon foot problem. However, it is not well understood and not often reported. Its clinical…
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