Bone Diseases, Developmental
"Bone Diseases, Developmental" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
No definition found.
Concept/Terms
Bone Diseases, Developmental- Bone Diseases, Developmental
- Bone Dysplasias
- Bone Dysplasia
- Dysplasia, Bone
- Dysplasias, Bone
- Developmental Bone Disease
- Bone Disease, Developmental
- Developmental Bone Diseases
Below are MeSH descriptors whose meaning is more general than "Bone Diseases, Developmental".
Below are MeSH descriptors whose meaning is more specific than "Bone Diseases, Developmental".
This graph shows the total number of publications written about "Bone Diseases, Developmental" by people in Harvard Catalyst Profiles by year, and whether "Bone Diseases, Developmental" was a major or minor topic of these publication.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1995 | 0 | 1 | 1 |
| 1996 | 3 | 0 | 3 |
| 1997 | 3 | 0 | 3 |
| 1998 | 1 | 0 | 1 |
| 1999 | 2 | 2 | 4 |
| 2000 | 1 | 2 | 3 |
| 2001 | 3 | 0 | 3 |
| 2003 | 1 | 0 | 1 |
| 2004 | 1 | 2 | 3 |
| 2005 | 2 | 0 | 2 |
| 2006 | 2 | 2 | 4 |
| 2007 | 3 | 1 | 4 |
| 2009 | 3 | 2 | 5 |
| 2010 | 1 | 1 | 2 |
| 2012 | 2 | 3 | 5 |
| 2013 | 6 | 0 | 6 |
| 2014 | 2 | 0 | 2 |
| 2015 | 3 | 1 | 4 |
| 2016 | 1 | 1 | 2 |
| 2017 | 5 | 1 | 6 |
| 2018 | 1 | 1 | 2 |
| 2019 | 2 | 0 | 2 |
| 2020 | 4 | 2 | 6 |
| 2021 | 1 | 0 | 1 |
| 2023 | 1 | 0 | 1 |
Below are the most recent publications written about "Bone Diseases, Developmental" by people in Profiles.
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Skeletal Dysplasia Families: A Stepwise Approach to Diagnosis. Radiographics. 2023 May; 43(5):e220067.
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High diagnostic yield in skeletal ciliopathies using massively parallel genome sequencing, structural variant screening and RNA analyses. J Hum Genet. 2021 Oct; 66(10):995-1008.
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Cancer risk in individuals with major birth defects: large Nordic population based case-control study among children, adolescents, and adults. BMJ. 2020 12 02; 371:m4060.
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PIGH deficiency can be associated with severe neurodevelopmental and skeletal manifestations. Clin Genet. 2021 02; 99(2):313-317.
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Development, behaviour and sensory processing in Marshall-Smith syndrome and Malan syndrome: phenotype comparison in two related syndromes. J Intellect Disabil Res. 2020 12; 64(12):956-969.
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Short Stature is Progressive in Patients with Heterozygous NPR2 Mutations. J Clin Endocrinol Metab. 2020 10 01; 105(10).
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Skeletal maturation and long-bone growth patterns of patients with progeria: a retrospective study. Lancet Child Adolesc Health. 2020 04; 4(4):281-289.
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Comprehensive clinically oriented workflow for nucleotide level resolution and interpretation in prenatal diagnosis of de novo apparently balanced chromosomal translocations in their genomic landscape. Hum Genet. 2020 Apr; 139(4):531-543.
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Slipped capital femoral epiphysis and Blount disease as indicators for early metabolic surgical intervention. Surg Obes Relat Dis. 2019 10; 15(10):1836-1841.
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Gain-of-function mutation of microRNA-140 in human skeletal dysplasia. Nat Med. 2019 04; 25(4):583-590.