PITUITARY DWARFISM I

Known as: PRIMORDIAL DWARFISM, IGHD1A, Isolated growth hormone deficiency, type 1b 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1961-2018
051019612018

Papers overview

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2014
2014
Primordial dwarfism (PD) is a disease in which severely impaired fetal growth persists throughout postnatal development and… (More)
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2014
2014
Structural maintenance of chromosomes (SMC) complexes are essential for maintaining chromatin structure and regulating gene… (More)
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2014
2014
BACKGROUND Primordial dwarfism (PD) is a heterogeneous clinical entity characterised by severe prenatal and postnatal growth… (More)
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2013
2013
Mutations in ORC1, ORC4, ORC6, CDT1, and CDC6, which encode proteins required for DNA replication origin licensing, cause Meier… (More)
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2013
2013
DNA double-strand break repair via non-homologous end joining (NHEJ) is involved in recombination of immunoglobulin and T-cell… (More)
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2009
2009
In their studies on the molecular basis of osteopoikilosis, Menten et al have identified three individuals with microdeletions on… (More)
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Highly Cited
2008
Highly Cited
2008
Fundamental processes influencing human growth can be revealed by studying extreme short stature. Using genetic linkage analysis… (More)
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1992
1992
At least three different sizes of GH-1 gene deletions (approximately 6.7, 7.0 and 7.6 kilobases) have been detected by Southern… (More)
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1990
1990
Familial isolated GH deficiency type 1A (IGHD1A) results from deletion of both GH alleles. To facilitate detection of cases of… (More)
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1982
1982
We describe three unrelated patients with intrauterine growth retardation (IUGR) and nearly identical bone changes. In certain… (More)
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