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Abnormality of the ribs
Known as:
Rib abnormalities
, Rib anomalies
An anomaly of the rib. [HPO:probinson]
National Institutes of Health
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Related topics
Related topics
9 relations
Alagille Syndrome 1
CHARGE Syndrome
Ichthyosis follicularis atrichia photophobia syndrome
Klippel-Feil deformity, conductive deafness, and absent vagina
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2013
2013
Nevoid basal cell carcinoma syndrome: a 40-year study in the South African population.
F. Titinchi
,
C. Nortjé
,
M. Parker
,
L. J. van Rensburg
Journal of Oral Pathology & Medicine
2013
Corpus ID: 23048963
BACKGROUND Nevoid basal cell carcinoma syndrome (NBCCS) is a hereditary autosomal dominant syndrome presenting with a number of…
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2010
2010
Segmental paternal uniparental disomy (patUPD) of 14q32 with abnormal methylation elicits the characteristic features of complete patUPD14
M. Irving
,
K. Buiting
,
+5 authors
R. Oakey
American Journal of Medical Genetics. Part A
2010
Corpus ID: 23483102
Uniparental disomy (UPD) for chromosome 14 is associated with well‐recognized phenotypes, depending on the parent of origin…
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Review
2007
Review
2007
Abnormal Rib Number in Childhood Malignancy: Implications for the Scoliosis Surgeon
R. Loder
,
G. Huffman
,
Eugene A Toney
,
L. Wurtz
,
R. Fallon
Spine
2007
Corpus ID: 13450160
Study Design. Retrospective review. Objective. To determine if rib anomalies are present in pediatric malignancies in the United…
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2006
2006
A spectrum of bronchopulmonary anomalies associated with tracheoesophageal malformations
J. Benson
,
M. Olsen
,
B. Fletcher
Pediatric Radiology
2006
Corpus ID: 23467527
The combination of tracheoesophageal and pulmonary malformations is unusual and reportedly carries a high mortality. We have…
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Review
2005
Review
2005
[Imaging features of neurofibromatosis type 1].
C. Jacques
,
J. Dietemann
Journal of neuroradiology. Journal de…
2005
Corpus ID: 25688121
Neurofibromatosis type 1 (NF1) is the most common of all the phakomatoses. It is an autosomal dominant disorder, with about 50…
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2005
2005
Prenatal infantile cortical hyperostosis (Caffey's disease): a ‘hepatic myeloid hyperplasia‐pulmonary hypoplasia sequence’ can explain the lethality of early onset cases
James R. Wright
,
M. C. Van den Hof
,
M. Macken
Prenatal Diagnosis
2005
Corpus ID: 24730390
Infantile cortical hyperostosis (ICH) is benign and self‐limiting when it presents near or after birth but is usually lethal when…
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Review
1999
Review
1999
Skeletal malformations associated with esophageal atresia: clinical and experimental studies.
H. Xia
,
L. Migliazza
,
S. Montedonico
,
J. Rodríguez
,
J. Diez-Pardo
,
J. Tovar
Journal of Pediatric Surgery
1999
Corpus ID: 19732446
1985
1985
CT Observation of Rib Abnormalities: Spectrum of Findings
G. Edelstein
,
Robert G
,
D. Slaker
,
W. Murphy
Journal of computer assisted tomography
1985
Corpus ID: 44789202
Surgicalhe CT studies in 63 patients in which rib abnormality was identified or excluded were retrospectively analyzed. The CT…
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1970
1970
Unilateral Raynaud's phenomenon caused by cervical-first rib anomalies.
N. W. Swinton
,
R. Hall
,
J. H. Baugh
,
H. A. Blake
American Journal of Medicine
1970
Corpus ID: 9562458
1963
1963
OVARIAN FIBROMAS AND MESENTERIC CYSTS: THEIR ASSOCIATION WITH HEREDITARY BASAL CELL CANCER OF THE SKIN.
W. Clendenning
,
T. Herd
,
J. Block
American Journal of Obstetrics and Gynecology
1963
Corpus ID: 42742187
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