Prenatal DNA analysis in four embryos/fetuses at risk of 21-hydroxylase deficiency (Q69929290)

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7 October 2019

title

Prenatal DNA analysis in four embryos/fetuses at risk of 21-hydroxylase deficiency (English)

1 reference

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7 October 2019

author name string

T Matsumoto

1

1 reference

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7 October 2019

T Kondoh

2

1 reference

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7 October 2019

T Kamei

3

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7 October 2019

M Yoshimoto

4

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7 October 2019

Y Tsuji

5

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7 October 2019

K Suzumori

6

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7 October 2019

R Izumi

7

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7 October 2019

N Iwatani

8

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7 October 2019

N Niikawa

9

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7 October 2019

publication date

1 December 1988

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European Journal of Pediatrics

7 October 2019

published in

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7 October 2019

volume

148

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7 October 2019

issue

3

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7 October 2019

page(s)

228-232

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The mutation and polymorphism of the human beta-globin gene and its surrounding DNA.

7 October 2019

cites work

1 reference

12 December 2020

Localization of the human prealbumin gene to 18p11.1-q12.3 by gene dose effect study of Southern blot hybridization

1 reference

12 December 2020

Complete nucleotide sequence of two steroid 21-hydroxylase genes tandemly arranged in human chromosome: a pseudogene and a genuine gene

1 reference

12 December 2020

Pharmacologic suppression of the fetal adrenal gland in utero. Attempted prevention of abnormal external genital masculinization in suspected congenital adrenal hyperplasia

1 reference

12 December 2020

Mapping of steroid 21-hydroxylase genes adjacent to complement component C4 genes in HLA, the major histocompatibility complex in man.

1 reference

12 December 2020

Late-onset form of congenital adrenal hyperplasia in the HLA-B14; DR1 haplotype is caused by a duplication in the 21-OH MHC gene region

1 reference

12 December 2020

Polymorphic DNA haplotypes at the human phenylalanine hydroxylase locus and their relationship with phenylketonuria

1 reference

12 December 2020

Associations between restriction fragment length polymorphisms detected with a probe for human 21-hydroxylase (21-OH) and two clinical forms of 21-OH deficiency

1 reference

12 December 2020

Prevalence of polymorphic 21-hydroxylase gene (CA21HB) mutations in salt-losing congenital adrenal hyperplasia.

1 reference

12 December 2020

Congenital adrenal hyperplasia (2).

1 reference

12 December 2020

First trimester prenatal diagnosis of 21-hydroxylase deficiency by linkage analysis to HLA-DNA probes and by 17-hydroxyprogesterone determination

1 reference

12 December 2020

Rearrangement of 21-hydroxylase genes in disease-associated MHC supratypes

1 reference

12 December 2020

Prenatal treatment of congenital adrenal hyperplasia resulting from 21-hydroxylase deficiency

1 reference

12 December 2020

Frequent deletion and duplication of the steroid 21-hydroxylase genes

1 reference

12 December 2020

Cloning and expression of cDNA encoding a bovine adrenal cytochrome P-450 specific for steroid 21-hydroxylation

1 reference

12 December 2020

Gene conversion in salt-losing congenital adrenal hyperplasia with absent complement C4B protein

1 reference

12 December 2020

Restriction maps and restriction fragment length polymorphisms of the human 21-hydroxylase genes.

1 reference

12 December 2020

HLA-linked congenital adrenal hyperplasia results from a defective gene encoding a cytochrome P-450 specific for steroid 21-hydroxylation

1 reference

12 December 2020

[HLA antigens and different clinical forms of 21-hydroxylase deficiency in the French population]

1 reference

12 December 2020

Two genes encoding steroid 21-hydroxylase are located near the genes encoding the fourth component of complement in man

1 reference

12 December 2020