Epiphyseal dysplasia

 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1951-2018
0102019512017

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Highly Cited
2001
Highly Cited
2001
Multiple epiphyseal dysplasia (MED) is a relatively mild and clinically variable osteochondrodysplasia, primarily characterized… (More)
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2001
2001
Multiple epiphyseal dysplasia (MED) is an autosomal dominantly inherited chondrodysplasia. It is clinically highly heterogeneous… (More)
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Highly Cited
2001
Highly Cited
2001
Mutations in type 3 repeats of cartilage oligomeric matrix protein (COMP) cause two skeletal dysplasias, pseudoachondroplasia… (More)
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Highly Cited
2001
Highly Cited
2001
Cartilage oligomeric matrix protein (COMP) and type IX collagen are key structural components of the cartilage extracellular… (More)
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Highly Cited
2000
Highly Cited
2000
Wolcott-Rallison syndrome (WRS) is a rare, autosomal recessive disorder characterized by permanent neonatal or early infancy… (More)
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1999
1999
Multiple epiphyseal dysplasia (MED), an autosomal dominant osteochondrodysplasia, is a clinically and genetically heterogeneous… (More)
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1999
1999
We have observed over 25 different mutations in the diastrophic dysplasia sulphate transporter gene (DTDST) in association with… (More)
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1998
1998
Pseudoachondroplasia (PSACH) and multiple epiphyseal dysplasia (MED) are autosomal dominant osteochondrodysplasias that result in… (More)
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Highly Cited
1995
Highly Cited
1995
Pseudoachondroplasia (PSACH) and multiple epiphyseal dysplasia (MED) are dominantly inherited chondrodysplasias characterized by… (More)
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Highly Cited
1986
Highly Cited
1986
More than 90% of patients with so-called primary or idiopathic osteoarthritis of the hips in whom sufficient data were available… (More)
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