About: Familial male pseudohermaphroditism with gynecomastia due to a testicular 17-ketosteroid reductase defect. I. Studies in vivo

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About: Familial male pseudohermaphroditism with gynecomastia due to a testicular 17-ketosteroid reductase defect. I. Studies in vivo Goto Sponge NotDistinct Permalink

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rdf:type	Item
description	artículu científicu (ast) wetenschappelijk artikel (nl) наукова стаття, опублікована в травні 1971 (uk) im Mai 1971 veröffentlichter wissenschaftlicher Artikel (de)
publication date	wds:Q57971915-D8844259-2A1F-4341-9644-5E922B67DF59
publication date	1971-05-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q57971915-8201BD9D-46DE-4C4A-AE51-DEEB74E7AD0E
language of work or name	English
author name string	wds:Q57971915-02C4F9D8-A2F8-48A8-91FE-C500C00AF905 wds:Q57971915-13DA7BC3-9419-4984-84D0-A6AD3740304E wds:Q57971915-1994DA96-6F29-49A9-87B9-9275881DB3F2 wds:Q57971915-41A089E8-459E-45DE-A338-CB216877385E wds:Q57971915-603831B2-9BB8-4E94-B13E-7775FC51AB95 wds:Q57971915-74529DBD-8BD5-410E-9BE7-35F8D586F297 wds:Q57971915-81CD83CF-EF5F-4201-8757-D3CD73EF98F1 wds:Q57971915-F65FF540-FF8C-4A9B-9E88-36422EBA1151 wds:Q57971915-F7C746E8-47D4-4A82-9C6C-475E8E119FCB wds:Q57971915-FA359B10-7513-4FF4-A2E1-DA0DB5AD7BDF
author name string	M David J Bertrand A M Morera A. M. MORERA E De Peretti E. DE PERETTI J M Saez J. BERTRAND J. M. SAEZ M. DAVID
rdfs:label	Familial male pseudohermaphroditism with gynecomastia due to a testicular 17-ketosteroid reductase defect. I. Studies in vivo (en) Familial male pseudohermaphroditism with gynecomastia due to a testicular 17-ketosteroid reductase defect. I. Studies in vivo (nl)
skos:prefLabel	Familial male pseudohermaphroditism with gynecomastia due to a testicular 17-ketosteroid reductase defect. I. Studies in vivo (en) Familial male pseudohermaphroditism with gynecomastia due to a testicular 17-ketosteroid reductase defect. I. Studies in vivo (nl)
name	Familial male pseudohermaphroditism with gynecomastia due to a testicular 17-ketosteroid reductase defect. I. Studies in vivo (en) Familial male pseudohermaphroditism with gynecomastia due to a testicular 17-ketosteroid reductase defect. I. Studies in vivo (nl)
title	wds:Q57971915-AFE4E177-4C02-4836-AEC2-867FA7400BD3 wds:Q57971915-E136B0ED-468C-4B13-834A-FAD1AE24ED95
title	Familial Male Pseudohermaphroditism with Gynecomastia Due to a Testicular 17-Ketosteroid Reductase Defect. I. Studiesin Vivo (en) Familial male pseudohermaphroditism with gynecomastia due to a testicular 17-ketosteroid reductase defect. I. Studies in vivo (en)
page(s)	wds:Q57971915-7DBD00E8-FCE5-45A4-AA93-E27231F07331 wds:Q57971915-B2FFAC8E-031E-44A8-9925-5F2A54D7C185
page(s)	604-610 604-10
instance of	wds:Q57971915-E5772CDF-28F2-4C0B-840C-A122DC18F196
instance of	scholarly article
PubMed ID	wds:Q57971915-DC5C80FB-3D98-4014-8B07-350B3C997E9D
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/4252809
PubMed ID	4252809
published in	wds:Q57971915-1AB6FE86-B8A0-40C8-89A3-24CDE3278779
published in	The Journal of Clinical Endocrinology and Metabolism
issue	wds:Q57971915-93C78657-B53E-40C8-AE85-85E74AA5CC6B
volume	wds:Q57971915-EA0D182E-C410-4093-A74B-B772DB3D6766
issue	5
volume	32
DOI	wds:Q57971915-AC2F5C10-EE36-4409-93F0-17545E3780BD
DOI	http://dx.doi.org/10.1210/JCEM-32-5-604
DOI	10.1210/JCEM-32-5-604
skos:altLabel	Familial Male Pseudohermaphroditism with Gynecomastia Due to a Testicular 17-Ketosteroid Reductase Defect. I. Studiesin Vivo (en) Familial Male Pseudohermaphroditism with Gynecomastia Due to a Testicular 17-Ketosteroid Reductase Defect. I. Studiesin Vivo (nl)
is owl:sameAs of	Familial male pseudohermaphroditism with gynecomastia due to a testicular 17-ketosteroid reductase defect. I. Studies in vivo
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q57971915
is cites work of	17beta-hydroxysteroid dehydrogenases: physiological roles in health and disease. Male pseudohermaphroditism with gynaecomastia due to testicular 17-ketosteroid reductase deficiency Dihydrotestosterone binding by cultured human fibroblasts. Comparison of cells from control subjects and from patients with hereditary male pseudohermaphroditism due to androgen resistance Genetic Disorders of Male Sexual Differentiation Physiology and molecular genetics of 17 beta-hydroxysteroid dehydrogenases A practical approach to intersex in the newborn period Natural potent androgens: lessons from human genetic models. Male pseudohermaphroditism: The complexities of male phenotypic development An etiologic and pathogenetic classification of male hermaphroditism 7 Gynaecomastia in male adolescents Male pseudohermaphroditism due to 17β-hydroxysteroid dehydrogenase deficiency: Studies on the natural history of the defect and effect of androgens on gender role 17beta-hydroxysteroid dehydrogenase 3 deficiency in a male pseudohermaphrodite Clinical, endocrine, and molecular findings in 17beta-hydroxysteroid dehydrogenase type 3 deficiency. XY females with enzyme deficiencies of steroid metabolism. A brief review Ten years experience with masculinizing genitoplasty in male pseudohermaphroditism due to 17 beta-hydroxysteroid dehydrogenase deficiency The child with ambiguous genitalia The diagnosis and management of intersex Endocrine studies in male pseudohermaphroditism in childhood and adolescence Male pseudohermaphroditism: genetics and clinical delineation Testicular function in post pubertal male pseudohermaphroditism Intersexuality and the diagnosis of gender identity disorder Ambiguous genitalia, small genitalia and undescended testes A practical approach to ambiguous genitalia in the newborn period Prepubertal male pseudohermaphroditism due to 17-ketosteroid reductase deficiency: diagnostic value of a hCG test and lack of HLA association Abnormalities of gonadal function in men 46,XY disorder of sex development due to 17-beta hydroxysteroid dehydrogenase type 3 deficiency in an infant of Greek origin. Endocrine findings in male pseudohermaphroditism The incomplete male Sexual Programing of the Rat Fetus and Neonate Studied by Selective Biochemical Testosterone-Depriving Agents Hormonal principles in normal and pathologic somatic sexual development Male hypogonadism. A Novel Mutation Causing 17-β-Hydroxysteroid Dehydrogenase Type 3 Deficiency in an Omani Child: First Case Report and Review of Literature Steroid enzyme defects leading to male pseudohermaphroditism Novel mutation among two sisters with 17β hydroxysteroid dehydrogenase type 3 deficiency Congenital adrenal hyperplasia The dilemma of the gender assignment in a Portuguese adolescent with disorder of sex development due to 17β-hydroxysteroid-dehydrogenase type 3 enzyme deficiency
is cites work of	wds:Q34242970-67A7FA71-4F76-4B62-BAF5-D55889BD4EC7 wds:Q70467427-9D8175B1-12E4-414F-9513-7ACA6DAD67A6 wds:Q67404260-A6521C52-3467-40AD-B32B-747A5E9761CC

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