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PROP1
LE WE PMID CA
PROP18556PROP1

11 hydoxylase

17 20 Desmolase

17 alpha hydroxylase 17 20 lyase

17 beta hydroxysteroid dehydrogenase

20 22 Desmolase

21 hydroxylase deficiency

3 beta hydroxysteroid dehydrogenase2

3 beta hydroxysteroid dehydrogenase3

5 alpha Reductase

Adrenal gland (Hyperplasia congenital)

AMH

AMHR2

Androgen insensitivity syndrome

Androgens (Hypogonadotropic hypogonadism)

Campomelic dysplasia

Congenital adrenal hyperplasia

CYP19A1 Aromatase

DAX1 NR0B1

Denys Drash syndrome

Folliculogenesis

Frasier s syndrome

GS alpha

Hedgehog

HESX1

HSD17B3

Hypophysis (Development)

Infertility

INSL3 Insulin like 3 Relaxin like factor

KAL

Kallmann s syndrome

Leptin

LHX3 Lim3

LHX4

McCune Albright syndrome

NR5A1 SF1

P450 side chain cleavage

PC1

Pituitary gland (Insufficiency Panhypopituitarism)

PROP1

Puberty (Delayed)

Puberty (Precocious)

Receptor (Androgen)

Receptor (Estrogen)

Receptor (FSH)

Receptor (Glucocorticoid)

Receptor (GnRH)

Receptor (LH)

SOX9

Spermatogenesis and spermatozoon

Sry

StAR

Steroid hormones (Synthesis)

Testis (Development)

WT1

2002  
1
Genetic causes of human reproductive disease.
[12050198] J Clin Endocrinol Metab 87(6): 2447-54 (2002)
2002  
2
Clinical review 148: Monogenic disorders of puberty.
[12050203] J Clin Endocrinol Metab 87(6): 2481-94 (2002)

Downloaded from http://www.kidney.de - The Database of Free Medical Reviews - The Metatextbook of Medicine - Ossip Groth

All Medline data shown were primarily retrieved from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.


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