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CYP21A2 Gene Mutations in Congenital Adrenal Hyperplasia: Genotype-phenotype correlation in Turkish children

45

Citations

55

References

2009

Year

Abstract

This is the first comprehensive study on the molecular basis of CAH patients in the Turkish population. Based on these results, we propose a modified screening strategy to facilitate molecular testing of CAH patients in our population.

References

YearCitations

2000

876

1992

580

1986

573

1986

527

1988

398

2000

389

1994

355

1995

304

1985

269

1991

207

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