Genetic Analysis of 21‐Hydroxylase Deficiency—Possible Role of Gene Conversion in Monogenic Disease—

Takehiko Sasazuki, Fumiki Harada

Research output: Contribution to journalArticle

Original languageEnglish
Pages (from-to)495-499
Number of pages5
JournalPediatrics International
Volume29
Issue number4
DOIs
Publication statusPublished - Jan 1 1987

Fingerprint

Gene Conversion
Congenital adrenal hyperplasia due to 21 hydroxylase deficiency

All Science Journal Classification (ASJC) codes

  • Pediatrics, Perinatology, and Child Health

Cite this

Genetic Analysis of 21‐Hydroxylase Deficiency—Possible Role of Gene Conversion in Monogenic Disease—. / Sasazuki, Takehiko; Harada, Fumiki.

In: Pediatrics International, Vol. 29, No. 4, 01.01.1987, p. 495-499.

Research output: Contribution to journalArticle

@article{fa0edd5433f340fdbc4fec661593fcee,
title = "Genetic Analysis of 21‐Hydroxylase Deficiency—Possible Role of Gene Conversion in Monogenic Disease—",
author = "Takehiko Sasazuki and Fumiki Harada",
year = "1987",
month = "1",
day = "1",
doi = "10.1111/j.1442-200X.1987.tb02226.x",
language = "English",
volume = "29",
pages = "495--499",
journal = "Pediatrics International",
issn = "1328-8067",
publisher = "Wiley-Blackwell",
number = "4",

}

TY - JOUR

T1 - Genetic Analysis of 21‐Hydroxylase Deficiency—Possible Role of Gene Conversion in Monogenic Disease—

AU - Sasazuki, Takehiko

AU - Harada, Fumiki

PY - 1987/1/1

Y1 - 1987/1/1

UR - http://www.scopus.com/inward/record.url?scp=84995007717&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=84995007717&partnerID=8YFLogxK

U2 - 10.1111/j.1442-200X.1987.tb02226.x

DO - 10.1111/j.1442-200X.1987.tb02226.x

M3 - Article

C2 - 3144881

AN - SCOPUS:84995007717

VL - 29

SP - 495

EP - 499

JO - Pediatrics International

JF - Pediatrics International

SN - 1328-8067

IS - 4

ER -