Publication | Open Access
A Chinese familial growth hormone deficiency with a deletion of 7.1 kb of DNA.
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Citations
11
References
1990
Year
Human GrowthAffected SibsGeneticsGenetic EpidemiologyPathologyMolecular GeneticsDisease Gene IdentificationNormal StatureEpigeneticsClinical GeneticsMendelian DisorderPublic HealthGrowth HormoneInherited Metabolic DiseaseStatistical GeneticsEndocrinologyChinese FamilyDevelopmental BiologyGenetic DisorderMedicine
Using restriction endonuclease analysis and a human growth hormone cDNA probe, we have found a Chinese family with a human growth hormone gene deletion. Two affected sibs are homozygous for a deletion of approximately 7.1 kb of DNA, which contains the normal human growth hormone gene. The patients' parents and grandmothers are heterozygous for the deleted gene. Their grandfathers are normal and homozygous for the hGH-N gene. All of them have normal stature.
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