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46XY siblings with inadequate virilization and CNS deficiency
R. P. Hoffman
, M. W. Steele
, P. A. Lee
, T. R. Brown
, S. L. Wenger
, P. L. Skiba
Department of Pediatrics
Division of Endocrinology
Research output
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Contribution to journal
›
Article
›
peer-review
5
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Scopus citations
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Keyphrases
Intellectual Disability
100%
Gonadotropins
100%
Virilization
100%
46,XY
100%
Hormone Levels
50%
Testosterone
50%
Luteinizing Hormone
50%
Multiple Congenital Anomalies
50%
Kindred
50%
Autosomal Dominant
50%
Steroidogenesis
50%
Human Chorionic Gonadotropin
50%
Androgen Insensitivity
50%
X-linked Disorder
50%
Seminiferous Tubules
50%
Gonadotropin Deficiency
50%
Facial Anomalies
50%
Ambiguous Genitalia
50%
Sex Limitation
50%
Micropenis
50%
Medicine and Dentistry
Virilization
100%
Congenital Malformation
50%
Hormone Determination
50%
Gonadotropin
50%
Autosomal Dominant Inheritance
50%
Steroidogenesis
50%
Karyotype
50%
Chorionic Gonadotropin
50%
Androgen Insensitivity Syndrome
50%
Luteinizing Hormone
50%
Face Malformation
50%
Seminiferous Tubule
50%
Ambiguous Genitalia
50%
Micropenis
50%
Pharmacology, Toxicology and Pharmaceutical Science
Virilization
100%
Gonadotropin
50%
Congenital Malformation
50%
Syndrome
50%
Luteinizing Hormone
50%
Chorionic Gonadotropin
50%
Androgen Insensitivity Syndrome
50%
Gonadotropin Deficiency
50%
Face Malformation
50%
Micropenis
50%
Ambiguous Genitalia
50%
Biochemistry, Genetics and Molecular Biology
Virilization
100%
Gonadotropin
100%
Karyotype
50%
Autosomal Dominant Inheritance
50%
Human Chorionic Gonadotropin
50%
Steroid Biosynthesis
50%
Seminiferous Tubule
50%
Luteinizing Hormone
50%