Molecular characterization in a case of isolated growth hormone deficiency and further prenatal diagnosis of an unborn sibling.
Indian J Hum Genet
; 2013 Oct-Dec ;19 (4): 475-478
Article
in En
| IMSEAR
| ID: sea-156618
Full text:
1
Index:
IMSEAR
Main subject:
Prenatal Diagnosis
/
Humans
/
Male
/
Polymerase Chain Reaction
/
Gene Deletion
/
Human Growth Hormone
/
Siblings
/
Fetus
/
Growth Disorders
/
Infant
Type of study:
Diagnostic_studies
/
Prognostic_studies
Language:
En
Journal:
Indian J Hum Genet
Year:
2013
Type:
Article