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Author:(In Bo OH)

1.A case of 46,XX/46,XX, del(3)(q21) mosaicism in amniocentesis: diagnostic problems and clinical significance.

Korean Journal of Obstetrics and Gynecology 1991;34(11):1619-1624

2.A study on chromosome mosaicism and pseudomosaicism in 4,376 amniocenteses.

Korean Journal of Obstetrics and Gynecology 1991;34(9):1201-1208

3.Prenatal diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

Journal of Korean Society of Endocrinology 1993;8(4):379-386

4.A case of successful transabdominal cervicoisthmic cercalge in a patient with incompetent internal os of cervix.

Bo Hoon OH ; Jung Hee CHIN

Korean Journal of Obstetrics and Gynecology 1991;34(7):1027-1033

5.Cytogenetic study of maker chromosome in amniocentesis.

Soo Yul BYUN ; Bo Hoon OH

Korean Journal of Obstetrics and Gynecology 1993;36(7):1275-1279

6.A case of 46,X del(X)(11.2).

Chang Hun KIM ; Bo Hoon OH

Korean Journal of Obstetrics and Gynecology 1993;36(7):1026-1032

7.Hormone profile in patients with simple virilizing congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

Jae Youl LEE ; Bo Hoon OH

Korean Journal of Obstetrics and Gynecology 1992;35(4):498-508

8.A case of 46,XX,18p-/46,XX,i(18q).

Rhi Ae JU ; Bo Hoon OH

Korean Journal of Obstetrics and Gynecology 1992;35(10):1551-1555

9.A case of consecutive famillial marker chromesome in amniocytes inherited from the father.

Kwang Hwi PARK ; Bo Hoon OH

Korean Journal of Obstetrics and Gynecology 1993;36(7):1683-1686

10.A case of 46,XX, del(18)(p11.1).

Jung Hee JIN ; Rhi Ae JU ; Bo Hoon OH

Korean Journal of Obstetrics and Gynecology 1992;35(9):1380-1382

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