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Broad palm
Known as:
Spade-like hand
, Spade-like hands
, Broad hand
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For children from birth to 4 years of age the palm width is more than 2 SD above the mean; for children from 4 to 16 years of age the palm width is…
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National Institutes of Health
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Related topics
Related topics
14 relations
Asphyxiating Thoracic Dystrophy 2
Bohring syndrome
Congenital spade-like hand
Dyggve-Melchior-Clausen syndrome
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
2019
Review
2019
Call a spade a spade: taxonomy and distribution of Pelobates, with description of a new Balkan endemic
C. Dufresnes
,
I. Strachinis
,
Elias Tzoras
,
S. Litvinchuk
,
Mathieu Denoël
ZooKeys
2019
Corpus ID: 197660507
Abstract The genomic era contributes to update the taxonomy of many debated terrestrial vertebrates. In an accompanying work, we…
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Review
2017
Review
2017
Pathophysiology, Diagnosis and Treatment of Somatosensory Tinnitus: A Scoping Review
H. Haider
,
D. Hoare
,
+7 authors
J. Paço
Frontiers in Neuroscience
2017
Corpus ID: 12739302
Somatosensory tinnitus is a generally agreed subtype of tinnitus that is associated with activation of the somatosensory…
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Review
2002
Review
2002
The Peters' plus syndrome: a review.
L. Maillette de Buy Wenniger‐Prick
,
R. Hennekam
Annales de Genetique
2002
Corpus ID: 22459565
1991
1991
Diagnostic hand anomalies in Smith-Magenis syndrome: four new patients with del (17)(p11.2p11.2)
Ikuko Kondo
,
Shinya Matsuura
,
+5 authors
Tadashi Kajii
American journal of medical genetics
1991
Corpus ID: 23415669
We report clinical and cytogenetic findings of 4 children (2 boys and 2 girls) with the Smith-Magenis syndrome. All 4 patients…
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Review
1991
Review
1991
Smith-Magenis syndrome: a new contiguous gene syndrome. Report of three new cases.
A. Moncla
,
M. Livet
,
M. Auger
,
J. Mattei
,
M. Mattei
,
F. Giraud
Journal of Medical Genetics
1991
Corpus ID: 16658378
Interstitial deletion of the short arm of chromosome 17 was detected in three patients. They all had a similar phenotype with…
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Review
1990
Review
1990
Five cases demonstrating the distinctive behavioural features of chromosome deletion 17(p 11.2 p 11.2) (Smith‐Magenis syndrome)
A. Colley
,
M. Leversha
,
L. Voullaire
,
J. Rogers
Journal of Paediatrics and Child Health
1990
Corpus ID: 27199100
Abstract Children with hyperactivity and self‐destructive behaviour present a difficult problem for parents and paediatricians…
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Highly Cited
1986
Highly Cited
1986
Interstitial deletion of (17)(p11.2p11.2): report of six additional patients with a new chromosome deletion syndrome.
R. Stratton
,
W. Dobyns
,
+10 authors
J. Reynolds
American journal of medical genetics
1986
Corpus ID: 23471597
Recently, a new clinically recognizable syndrome resulting from a small interstitial deletion of 17p [del(17)(p11.2p11.2)] was…
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1975
1975
The inheritance of the Aarskog facial-digital-genital syndrome.
P. Berman
,
Claude Desjardins
,
F. Fraser
Jornal de Pediatria
1975
Corpus ID: 13596097
Highly Cited
1973
Highly Cited
1973
Dentoalveolar morphology and developmental changes in Down's syndrome (trisomy 21).
G. M. Jensen
,
J. Cleall
,
A. Yip
American Journal of Orthodontics
1973
Corpus ID: 7507816
1972
1972
The Aarskog syndrome.
C. T. Furukawa
,
B. Hall
,
David W. Smith
Jornal de Pediatria
1972
Corpus ID: 29009732
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