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Amelia
Known as:
Amelia of unspecified limb
, Congenital absence of limb NOS
A congenital malformation characterized by the complete absence of all limbs.
National Institutes of Health
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Related topics
Related topics
9 relations
Congenital absence
Congenital musculoskeletal anomalies
Ectromelia
Hemimelia
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Broader (2)
Fetal Diseases
Musculoskeletal Diseases
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2010
2010
Fetal malformations and early embryonic gene expression response in cynomolgus monkeys maternally exposed to thalidomide.
M. Ema
,
Ryota Ise
,
+6 authors
T. Ihara
Reproductive Toxicology
2010
Corpus ID: 24623524
2009
2009
Detection of continuous erythropoietin receptor activator in blood and urine in anti-doping control
F. Lasne
,
Laurent Martin
,
Jean-Antoine Martin
,
J. de Ceaurriz
Haematologica
2009
Corpus ID: 207573465
Anti-doping control of erythropoietin (Epo) relies on the differentiation by isoelectric profile of natural endogenous hormone…
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Highly Cited
2008
Highly Cited
2008
Unpacking science for all through the lens of identities-in-practice: the stories of Amelia and Ginny
Edna Tan
,
Angela Calabrese Barton
2008
Corpus ID: 35433549
This manuscript reports on an ethnographic study of two Latina students who attended an urban middle school in a low-income…
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Review
1994
Review
1994
Congenital abnormalities associated with limb deficiency defects: a population study based on cases from the Hungarian Congenital Malformation Registry (1975-1984).
J. Evans
,
M. Vitéz
,
A. Czeizel
American journal of medical genetics
1994
Corpus ID: 10950012
Limb deficiency defects (LD) occurring among 1,575,904 births in Hungary during 1975-1984 were reviewed. The overall birth…
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1991
1991
Bilateral split hand and split foot malformation in a boy with a de novo interstitial deletion of 7q21.3
S. Roberts
,
H. Hughes
,
S. Davies
,
A. Meredith
Journal of Medical Genetics
1991
Corpus ID: 27926833
A case of bilateral split hand and split foot malformation is reported in a boy with a complex rearrangement of chromosome 7…
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Review
1990
Review
1990
Ectro-amelia syndrome associated with an interstitial deletion of 7q.
Martha A. Morey
,
Rodney R. Higgins
American journal of medical genetics
1990
Corpus ID: 34731399
We describe a premature male infant with an interstitial deletion of 7q [46,XY,del(7) (pter----q21.3::q31.3----qter…
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Highly Cited
1990
Highly Cited
1990
Amelia: incidence and associated defects in a large population.
U. Froster-Iskenius
,
P. Baird
Teratology
1990
Corpus ID: 35640963
Amelia, or complete absence of a limb, is a very rare congenital anomaly. The incidence of amelia in a population of 1,213,913…
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1990
1990
Roberts syndrome or "X-linked amelia"?
R. Gershoni-baruch
,
A. Drugan
,
M. Bronshtein
,
E. Zimmer
American journal of medical genetics
1990
Corpus ID: 19133366
We report on a syndrome of tetra-amelia, facial clefts, absence of ears, nose, and atresia ani, affecting 7 male infants or…
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Highly Cited
1984
Highly Cited
1984
Infants with congenital limb reduction registered in the Swedish Register of Congenital Malformations.
B. Källén
,
T. Rahmani
,
J. Winberg
Teratology
1984
Corpus ID: 27212292
Limb reduction defects reported to the Swedish Register of Congenital Malformations 1965-1979 have been analyzed from a…
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1965
1965
A SYSTEM OF POWERED PROSTHESES FOR SEVERE BILATERAL UPPER LIMB DEFICIENCY.
D. Simpson
,
D. Lamb
Journal of Bone and Joint Surgery-british Volume
1965
Corpus ID: 46501075
1. A description of the planning for the application of a powered prosthesis to a child with bilateral upper limb deficiency is…
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