Male Pseudohermaphroditism Due to 17 β-Hydroxysteroid Dehydrogenase Deficiency (17 βHSD) in a Large Arab Kinship. Studies on the Natural History of the Defect

G. Kohn,; E.E. Lasch,; R. El Shawwa,; Y. Litvin,; A. Rosler,

doi:10.1515/JPEM.1985.1.1.29

Home Medicine Male Pseudohermaphroditism Due to 17 β-Hydroxysteroid Dehydrogenase Deficiency (17 βHSD) in a Large Arab Kinship. Studies on the Natural History of the Defect

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Male Pseudohermaphroditism Due to 17 β-Hydroxysteroid Dehydrogenase Deficiency (17 βHSD) in a Large Arab Kinship. Studies on the Natural History of the Defect

G. Kohn, , E.E. Lasch, , R. El Shawwa, , Y. Litvin, and A. Rosler,

Published/Copyright: January 1, 1985

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From the journal Journal of Pediatric Endocrinology and Metabolism Volume 1 Issue 1

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Kohn,, G., Lasch,, E.E., El Shawwa,, R., Litvin,, Y. and Rosler,, A.. "Male Pseudohermaphroditism Due to 17 β-Hydroxysteroid Dehydrogenase Deficiency (17 βHSD) in a Large Arab Kinship. Studies on the Natural History of the Defect" Journal of Pediatric Endocrinology and Metabolism, vol. 1, no. 1, pp. 29-38. https://doi.org/10.1515/JPEM.1985.1.1.29

Kohn,, G., Lasch,, E., El Shawwa,, R., Litvin,, Y. & Rosler,, A. (). Male Pseudohermaphroditism Due to 17 β-Hydroxysteroid Dehydrogenase Deficiency (17 βHSD) in a Large Arab Kinship. Studies on the Natural History of the Defect. Journal of Pediatric Endocrinology and Metabolism, 1(1), 29-38. https://doi.org/10.1515/JPEM.1985.1.1.29

Kohn,, G., Lasch,, E., El Shawwa,, R., Litvin,, Y. and Rosler,, A. () Male Pseudohermaphroditism Due to 17 β-Hydroxysteroid Dehydrogenase Deficiency (17 βHSD) in a Large Arab Kinship. Studies on the Natural History of the Defect. Journal of Pediatric Endocrinology and Metabolism, Vol. 1 (Issue 1), pp. 29-38. https://doi.org/10.1515/JPEM.1985.1.1.29

Kohn,, G., Lasch,, E.E., El Shawwa,, R., Litvin,, Y. and Rosler,, A.. "Male Pseudohermaphroditism Due to 17 β-Hydroxysteroid Dehydrogenase Deficiency (17 βHSD) in a Large Arab Kinship. Studies on the Natural History of the Defect" Journal of Pediatric Endocrinology and Metabolism 1, no. 1 (): 29-38. https://doi.org/10.1515/JPEM.1985.1.1.29

Kohn, G, Lasch, E, El Shawwa, R, Litvin, Y, Rosler, A. Male Pseudohermaphroditism Due to 17 β-Hydroxysteroid Dehydrogenase Deficiency (17 βHSD) in a Large Arab Kinship. Studies on the Natural History of the Defect. Journal of Pediatric Endocrinology and Metabolism. ;1(1): 29-38. https://doi.org/10.1515/JPEM.1985.1.1.29

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TABLE OF CONTENTS
Notes on the Biology of Η-Y Antigen
The Interrelationships Between Testosterone and Zinc Metabolism
Recent Advances in Treatment of the Glycogenoses
Male Pseudohermaphroditism Due to 17 β-Hydroxysteroid Dehydrogenase Deficiency (17 βHSD) in a Large Arab Kinship. Studies on the Natural History of the Defect
Hyperinsulinemic Hypoglycemia of Infancy: Attempted Therapy with Streptozotocin
Familial Aggregation of Hashimoto's Thyroiditis and Studies of HLA Typing
Diazoxide Treatment of Neonatal and Infant Hypoglycemia: A Review and Reassessment
Paradoxical Association of Central Precocious Puberty and Hypergonadotropic Hypogonadism in 3 Patients with Klinefelter, Down, and Turner Syndrome

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https://doi.org/10.1515/JPEM.1985.1.1.29

Articles in the same Issue

TABLE OF CONTENTS
Notes on the Biology of Η-Y Antigen
The Interrelationships Between Testosterone and Zinc Metabolism
Recent Advances in Treatment of the Glycogenoses
Male Pseudohermaphroditism Due to 17 β-Hydroxysteroid Dehydrogenase Deficiency (17 βHSD) in a Large Arab Kinship. Studies on the Natural History of the Defect
Hyperinsulinemic Hypoglycemia of Infancy: Attempted Therapy with Streptozotocin
Familial Aggregation of Hashimoto's Thyroiditis and Studies of HLA Typing
Diazoxide Treatment of Neonatal and Infant Hypoglycemia: A Review and Reassessment
Paradoxical Association of Central Precocious Puberty and Hypergonadotropic Hypogonadism in 3 Patients with Klinefelter, Down, and Turner Syndrome