FAQ

Structure of fontanel of skull

Known as: Set of fontanelles, Fontanelle, Fontanelles 
The four gaps in the skull of a neonate or fetus where the sutures converge. The bulging or depression of the membranous soft spots can be indicative… (More)
National Institutes of Health

Topic mentions per year

Topic mentions per year

1936-2017
0204019362016

Related topics

Related topics

6 relations
Body partBone structure of craniumFetal SkullPediatric Terminology

Narrower (2)

Mastoid FontanelleStructure of anterior fontanel of skull

Related mentions per year

Related mentions per year

1936-2018
19401960198020002020
Structure of fontanel of skull
Bone structure of cranium
Body part
Structure of anterior fontanel of skull
Pediatric Terminology
Fetal Skull

Papers overview

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Highly Cited
2010
Highly Cited
2010
The p38 MAPK pathway is essential for skeletogenesis and bone homeostasis in mice.
Nearly every extracellular ligand that has been found to play a role in regulating bone biology acts, at least in part, through… (More)
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2009
2009
Mutations in LTBP4 cause a syndrome of impaired pulmonary, gastrointestinal, genitourinary, musculoskeletal, and dermal development.
We report recessive mutations in the gene for the latent transforming growth factor-beta binding protein 4 (LTBP4) in four… (More)
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2003
2003
Treatment of term infants with head cooling and mild systemic hypothermia (35.0 degrees C and 34.5 degrees C) after perinatal asphyxia.
OBJECTIVE To assess the safety of selective head cooling in birth-asphyxiated term newborn infants while maintaining the rectal… (More)
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2002
2002
Functional analysis of RUNX2 mutations in Japanese patients with cleidocranial dysplasia demonstrates novel genotype-phenotype correlations.
Cleidocranial dysplasia (CCD) is an autosomal dominant heritable skeletal disease caused by heterozygous mutations in the… (More)
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1999
1999
Mutation analysis of core binding factor A1 in patients with cleidocranial dysplasia.
Cleidocranial dysplasia (CCD) is a dominantly inherited disorder characterized by patent fontanelles, wide cranial sutures… (More)
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Highly Cited
1997
Highly Cited
1997
Mutations Involving the Transcription Factor CBFA1 Cause Cleidocranial Dysplasia
Cleidocranial dysplasia (CCD) is an autosomal-dominant condition characterized by hypoplasia/aplasia of clavicles, patent… (More)
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Highly Cited
1997
Highly Cited
1997
Missense mutations abolishing DNA binding of the osteoblast-specific transcription factor OSF2/CBFA1 in cleidocranial dysplasia
Cleidocranial dysplasia (CCD) is an autosomal dominant disorder characterized by hypoplastic or absent clavicles, large… (More)
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Highly Cited
1997
Highly Cited
1997
Chromosome 1p36 deletions: the clinical phenotype and molecular characterization of a common newly delineated syndrome.
Deletions of the distal short arm of chromosome 1 (1p36) represent a common, newly delineated deletion syndrome, characterized by… (More)
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Highly Cited
1986
Highly Cited
1986
Endoscopic endonasal surgery--concepts in treatment of recurring rhinosinusitis. Part II. Surgical technique.
Our endoscopic endonasal surgery, under the guidance of rigid endoscopes, aims at the primary focuses in the anterior ethmoid… (More)
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Highly Cited
1980
Highly Cited
1980
Vitamin D supplements in pregnant Asian women: effects on calcium status and fetal growth.
In a double-blind trial of vitamin D supplements in pregnant Asian women calciferol (ergocalciferol, 1000 IU/day) was… (More)
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