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Phalanx of hand
Known as:
Phalanges, Finger
, Phalanges
, phalanx hand
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Bones that make up the SKELETON of the FINGERS, consisting of two for the THUMB, and three for each of the other fingers.
National Institutes of Health
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Related topics
Related topics
25 relations
Blood supply aspects
Body part
Bone structure of phalanx of foot
Bone structure of upper limb
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Broader (3)
Bone structure of hand
Phalanx Unspecified
Structure of long bone
Narrower (5)
Bone structure of phalanx of thumb
Distal phalanx of hand
Proximal phalanx of finger
Structure of phalanx of middle finger
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2007
Highly Cited
2007
Life-history traits in green toad (Bufo viridis) populations: indicators of habitat quality
U. Sinsch
,
C. Leskovar
,
Anja DrobigA. Drobig
,
A. König
,
W. Grosse
2007
Corpus ID: 55767468
Five life-history traits (age and size at maturity, longevity, potential reproductive life span, age-dependent growth rate) were…
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Review
2006
Review
2006
Malunions of the finger metacarpals and phalanges.
A. Freeland**
,
S. Lindley
Hand Clinics
2006
Corpus ID: 29938261
2000
2000
Prediction of bone strength of distal forearm using radius bone mineral density and phalangeal speed of sound.
C. Wu
,
D. Hans
,
+5 authors
H. Genant
Bone
2000
Corpus ID: 31050154
1999
1999
Phalangeal morphology of the paromomyidae (?primates, plesiadapiformes): the evidence for gliding behavior reconsidered.
M. Hamrick
,
Burt A. Rosenman
,
Jason A. Brush
American Journal of Physical Anthropology
1999
Corpus ID: 42321315
A comparative morphometric analysis of isolated proximal and intermediate phalanges attributed to the paromomyids Ignacius…
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Highly Cited
1998
Highly Cited
1998
A new spontaneous mouse mutation of Hoxd13 with a polyalanine expansion and phenotype similar to human synpolydactyly.
K. Johnson
,
H. Sweet
,
L. Donahue
,
P. Ward-Bailey
,
R. Bronson
,
M. Davisson
Human Molecular Genetics
1998
Corpus ID: 43001069
Human synpolydactyly (SPD) is an inherited congenital limb malformation caused by mutations in the HOXD13 gene. Heterozygotes are…
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1998
1998
Grebe syndrome: clinical and radiographic findings in affected individuals and heterozygous carriers.
Teresa Costa
,
Gale R. Ramsby
,
+5 authors
Petros Tsipouras
American journal of medical genetics
1998
Corpus ID: 23363865
Grebe syndrome is a recessively inherited acromesomelic dysplasia. We studied, clinically and radiographically, 10 affected…
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1990
1990
Skeletal development of the striped dolphin(Stenella coeruleoalba)in Japanese waters
Haruka Ito
,
N. Miyazaki
1990
Corpus ID: 83789203
Development, sexual dimorphisms and individual differences of the skele ton of the striped dolphin (Stenella coeruleoalba) living…
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1989
1989
Spatial and temporal expression pattern of retinoic acid receptor genes during mouse bone development
S. Noji
,
T. Yamaai
,
E. Koyama
,
T. Nohno
,
S. Taniguchi
FEBS Letters
1989
Corpus ID: 40012395
Review
1986
Review
1986
Ultrasound Examination of Skin Thickness in Patients with Progressive Systemic Sclerosis (Scleroderma)
A. Åkesson
,
L. Forsberg
,
E. Hederström
,
F. Wollheim
Acta radiologica: diagnosis
1986
Corpus ID: 43842213
A new ultrasound technique for measuring skin thickness in 40 patients with progressive systemic sclerosis (scleroderma) and in…
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1973
1973
Congenital diplopodia with hypoplasia or aplasia of the tibia. A report of six cases.
K. Karchinov
Journal of Bone and Joint Surgery-british Volume
1973
Corpus ID: 20294344
1. The syndrome here described in six Bulgarian subjects is characterised by partial duplication of the foot or diplopodia…
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