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Clinodactyly
Known as:
Finger clinodactyly
An angulation of a digit at an interphalangeal joint in the plane of the palm (finger) or sole (toe). [pmid:16252026]
National Institutes of Health
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Related topics
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50 relations
AMINOPTERIN SYNDROME SINE AMINOPTERIN
Aarskog syndrome
Blepharo-cheilo-dontic syndrome
Brachydactyly, Type A1, B
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2012
2012
Mosaic ring chromosome 21, monosomy 21, and isodicentric ring chromosome 21: prenatal diagnosis, molecular cytogenetic characterization, and association with 2-Mb deletion of 21q21.1-q21.2 and 5-Mb…
Chih-ping Chen
,
Yi-Hui Lin
,
+6 authors
Wayseen Wang
Taiwanese Journal of Obstetrics & Gynecology
2012
Corpus ID: 205417498
2009
2009
Foot or hand malformations related to deep venous system anomalies of the lower limb in Klippel-Trénaunay syndrome.
P. Redondo
,
G. Bastarrika
,
+4 authors
A. Alonso-Burgos
Journal of American Academy of Dermatology
2009
Corpus ID: 26054994
2009
2009
Screening for genomic variants in ZFP57 in Silver-Russell syndrome patients with 11p15 epimutations.
S. Spengler
,
Magdalena Gogiel
,
N. Schönherr
,
G. Binder
,
T. Eggermann
European Journal of Medical Genetics
2009
Corpus ID: 33403032
2009
2009
An interstitial deletion of 7.1Mb in chromosome band 6p22.3 associated with developmental delay and dysmorphic features including heart defects, short neck, and eye abnormalities.
A. Bremer
,
J. Schoumans
,
M. Nordenskjöld
,
B. Anderlid
,
M. Giacobini
European Journal of Medical Genetics
2009
Corpus ID: 6978673
Review
2008
Review
2008
Catel-Manzke syndrome: two new patients and a critical review of the literature.
H. Manzke
,
K. Lehmann
,
E. Klopocki
,
A. Caliebe
European Journal of Medical Genetics
2008
Corpus ID: 34104086
2005
2005
Short QT syndrome or Andersen syndrome: Yin and Yang of Kir2.1 channel dysfunction.
E. Schulze-Bahr
Circulation Research
2005
Corpus ID: 5662611
See related article, pages 800–807 In 1994, the complete human cDNA of an inwardly rectifying K+ channel gene, KCNJ2 or Kir2.1…
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2003
2003
Mosaicism del(8p)/inv dup(8p) in a dysmorphic female infant: a mosaic formed by a meiotic error at the 8p OR gene and an independent terminal deletion event
J. Vermeesch
,
R. Thoelen
,
I. Salden
,
M. Raes
,
G. Matthijs
,
J. Fryns
Journal of Medical Genetics
2003
Corpus ID: 8112903
Various chromosomal rearrangements are associated with the distal 8p region. Among them are the inv dup(8p),1 del(8p22),2–5 and…
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2000
2000
Bloom's syndrome–‐a first report from India
B. Reddy
,
A. Kochhar
,
M. Anitha
,
Ramesh Bamezai
International Journal of Dermatology
2000
Corpus ID: 21294482
A 6‐year‐old boy presented with complaints of redness and scarring over the face to the outpatient clinic of the Dermatology…
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Review
1996
Review
1996
Odontodysplasia, gingival manifestations, and accompanying abnormalities.
K. Fanibunda
,
J. Soames
Oral surgery, oral medicine, oral pathology, oral…
1996
Corpus ID: 22749800
1992
1992
Mental retardation with blepharo‐naso‐facial abnormalities and hand malformations: a new syndrome?
L. Maldergem
,
C. Wetzburger
,
A. Verloes
,
C. Fourneau
,
Y. Gillerot
Clinical Genetics
1992
Corpus ID: 10817955
Van Maldergem L, Wetzburger C, Verloes A, Fourneau C, Gillerot Y. Mental retardation with blepharo‐naso‐facial abnormalities and…
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