(Q72030098)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6948766%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

title

HLA genotypes and HLA-linked genetic markers in Italian patients with classical 21-hydroxylase deficiency (English)

1 reference

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23 October 2019

10

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23 October 2019

author name string

M S Pollack

1

1 reference

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23 October 2019

M I New

2

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23 October 2019

G J O'Neill

3

1 reference

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23 October 2019

L S Levine

4

1 reference

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23 October 2019

C Callaway

5

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23 October 2019

S Pang

6

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23 October 2019

E Cacciari

7

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23 October 2019

F Mantero

8

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23 October 2019

A Cassio

9

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23 October 2019

G Chiumello

11

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23 October 2019

G F Rondanini

12

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23 October 2019

L Gargantini

13

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23 October 2019

G Giovannelli

14

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23 October 2019

R Virdis

15

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23 October 2019

E Bartolotta

16

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23 October 2019

C Migliori

17

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23 October 2019

C Pintor

18

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23 October 2019

L Tato

19

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23 October 2019

F Barboni

20

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23 October 2019

B Dupont

21

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23 October 2019

publication date

1 January 1981

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23 October 2019

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23 October 2019

volume

58

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23 October 2019

issue

3

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23 October 2019

page(s)

331-337

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https://scigraph.springernature.com/pub.10.1007/bf00294933

23 October 2019

exact match

0 references

cites work

Cryptic 21-hydroxylase deficiency in families of patients with classical congenital adrenal hyperplasia.

1 reference

12 December 2020

HLA linkage and B14, DR1, BfS haplotype association with the genes for late onset and cryptic 21-hydroxylase deficiency

1 reference

12 December 2020

Microfilter paper method for 17 alpha-hydroxyprogesterone radioimmunoassay: its application for rapid screening for congenital adrenal hyperplasia

1 reference

12 December 2020

HLA-A, B, C, DR alleles in congenital adrenal hyperplasia

1 reference

12 December 2020

Sequential tests for the detection of linkage

1 reference

12 December 2020

Late onset 21-hydroxylase deficiency and HLA in the Ashkenazi population: A new Allele at the 21-hydroxylase locus

1 reference

12 December 2020

Genetics of acquired and congenital adrenal hyperplasia

1 reference

12 December 2020

Hormonal Phenotype and HLA-Genotype in Families of Patients with Congenital Adrenal Hyperplasia (21-Hydroxylase Deficiency)

1 reference

12 December 2020

1 reference

12 December 2020

Possible genetic linkage disequilibrium between HLA and the 21-hydroxylase deficiency gene (congenital adrenal hyperplasia)

1 reference

12 December 2020

Gene frequencies and genetic linkage disequilibrium for the HLA-linked genes Bf, C2, C4S, C4F, 21-hydroxylase deficiency, and glyoxalase I

1 reference

12 December 2020

Detection of heterozygote of 21-hydroxylase deficiency

1 reference

12 December 2020

Genetic polymorphism in human glycine-rich beta-glycoprotein

1 reference

12 December 2020

Genetic mapping of the 21-hydroxylase-deficiency gene within the HLA linkage group

1 reference

12 December 2020

Properdin factor B polymorphism in continental Italy and Sardinia

1 reference

12 December 2020

Structural heterogeneity of C2 Complement protein and its genetic variants in man: a new polymorphism of the HLA region

1 reference

12 December 2020

Close genetic linkage between HLA and congenital adrenal hyperplasia (21-hydroxylase deficiency).

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00294933

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6948766%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

1 reference