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Abnormality of calvarial morphology
Known as:
Abnormality of the shape of cranium
, Abnormally shaped skull
, Abnormality of cranial bone morphology
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The presence of an abnormal shape of the calvaria (skullcap), that is, of that part of the skull that is made up of the superior portions of the…
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National Institutes of Health
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2016
2016
Posterior calvarial osseodistraction for syndromic craniosynostosis
N. Opie
,
M. Evans
2016
Corpus ID: 79022982
2014
2014
The evolution of a new Craniofacial Procedure: From Concept to established Intervention. The 8 year history of Posterior Calvarial Osseodistraction and its use in Craniofacial Surgery
M. Evans
,
M. Dover
,
H. Nishkawa
,
D. Rodrigues
,
N. White
2014
Corpus ID: 71361938
2006
2006
Predicting Neuropsychological Development from Skull Imaging
H. J. Lin
,
S. Ruiz-Correa
,
L. Shapiro
,
M. Speltz
,
M. Cunningham
,
R. Sze
Annual International Conference of the IEEE…
2006
Corpus ID: 564770
Craniosynostosis is a serious and common pediatric disease caused by the premature fusion of sutures of the skull. Although…
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Review
1996
Review
1996
Interstitial deletion of the short arm of chromosome 10: Report of a case and review of the literature
Zenichiro Kato
,
Tomomi Kato
,
N. Kondo
,
T. Orii
The Japanese Journal of Human Genetics
1996
Corpus ID: 24277938
SummaryThe fifth patient with an interstitial deletion of the short arm of chromosome 10 is described. She showed most of the…
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1996
1996
Suture formation, premature sutural fusion, and suture default zones in Apert syndrome.
M. Michael Cohen
,
Sven Kreiborg
American journal of medical genetics
1996
Corpus ID: 24675104
On the basis of our studies, we postulate that suture formation in Apert syndrome is related to the relative maturity of abutting…
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1992
1992
Partial deletion 10p syndrome. Report of two patients.
M. G. Obregon
,
R. Mingarelli
,
A. Giannotti
,
A. Di comite
,
F. Spedicato
,
B. Dallapiccola
Annales de Genetique
1992
Corpus ID: 42560303
Two patients with partial deletion of the short arm of chromosome 10 are described. They showed most of the features observed in…
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1986
1986
Very low birthweight and normal birthweight infants: A comparison of continuing morbidity
G. Ford
,
A. Rickards
,
W. Kitchen
,
J. Lissenden
,
M. Ryan
,
C. Keith
Medical Journal of Australia
1986
Corpus ID: 33695354
One hundred and forty‐eight (95.5%) of 155 consecutive two‐year survivors of 227 very low birthweight (VLBW, less than 1501 g…
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1983
1983
Prenatal diagnosis of perinatally lethal osteogenesis imperfecta.
B. R. Elejalde
,
M. de Elejalde
,
J. M. Opitz
American journal of medical genetics
1983
Corpus ID: 1341251
Prenatal diagnosis of osteogenesis imperfecta was achieved at 17 weeks of gestation using ultrasound through recognition of low…
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1964
1964
A CASE OF TRISOMY 16-18 SYNDROME. SPECULATION ON PATHOGENESIS OF CHROMOSOME-INDUCED MALFORMATIONS.
A. Levkoff
,
G. Mather
,
R. Eisenstein
A M A Journal of Diseases of Children
1964
Corpus ID: 34088978
Over 30 cases of group 16-18 trisomy syndrome have been reported. The most common defects are summarized in the Table. Included…
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