Results 141 to 150 of about 2,046,767 (198)
Polymorphism analysis of estrogen receptor β Gene RsaI and AluI in girls with idiopathic central precocious puberty: investigating the relationship and implications for early risk prediction. [PDF]
Front Endocrinol (Lausanne)Liu P +5 more
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Precocious puberty in boys: current insights into etiology, genetic advances, and environmental factors. [PDF]
Front Endocrinol (Lausanne)Amodeo ME +3 more
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Embryonic origin of XX/XY chimerism in an in vitro fertilization-conceived individual. [PDF]
F S RepPatel A +3 more
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INHAND: Non-proliferative and proliferative lesions of fish - Chapter 9. Fish female reproductive system. [PDF]
J Toxicol PatholBaumgartner W +13 more
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Gynaecologia, 2010
Mixed gonadal dysgenesis is a condition characterised by presence of a testis on one side and a streak gonad on the other. Two such patients with the condition are described, one with a predominantly female external genitalia and the other with predominantly male external genitalia. The former was a mosaic of XO deleted Y, while the latter was XY.
J, Janata, M, Krecek, L, Stárka
openaire +3 more sources
Mixed gonadal dysgenesis is a condition characterised by presence of a testis on one side and a streak gonad on the other. Two such patients with the condition are described, one with a predominantly female external genitalia and the other with predominantly male external genitalia. The former was a mosaic of XO deleted Y, while the latter was XY.
J, Janata, M, Krecek, L, Stárka
openaire +3 more sources
Pediatrics, 1973
The syndrome of mixed gonadal dysgenesis (MGD) is characterized by a unilateral testis, usually intra-abdominal, a streak gonad on the contralateral side, and persistent Mullerian structures. The external genitalia are always masculinized to some extent, on occasion achieveing a normal male phenotype: the somatic signs of Turner's syndrome are ...
Daniel D Federman, Frank Davidoff
exaly +3 more sources
The syndrome of mixed gonadal dysgenesis (MGD) is characterized by a unilateral testis, usually intra-abdominal, a streak gonad on the contralateral side, and persistent Mullerian structures. The external genitalia are always masculinized to some extent, on occasion achieveing a normal male phenotype: the somatic signs of Turner's syndrome are ...
Daniel D Federman, Frank Davidoff
exaly +3 more sources
Acta Endocrinologica, 1975
Mixed gonadal dysgenesis (MCG) is a rare intersexual disorder, characterized in most cases by the presence of a testis and a contralateral streak gonad; in some cases the contralateral gonad may be rudimentary not having differentiated into an ovary or into a testis and in other cases it may be absent.
W, Zäh, A E, Kalderon, J R, Tucci
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Mixed gonadal dysgenesis (MCG) is a rare intersexual disorder, characterized in most cases by the presence of a testis and a contralateral streak gonad; in some cases the contralateral gonad may be rudimentary not having differentiated into an ovary or into a testis and in other cases it may be absent.
W, Zäh, A E, Kalderon, J R, Tucci
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Clinical Pediatrics, 1974
An apparently female child was found to have ambiguous genitalia with an enlarged phallus. The sex chromatin was negative. Cultured leuko cytes showed XY karyotype. At laparotomy, a uterus with normal fallopian tubes was found. An intra-abdominal testis on one side and a streak gonad on the other side were also detected, and confirmed by histologic ...
N, Gadoth, S W, Moses
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An apparently female child was found to have ambiguous genitalia with an enlarged phallus. The sex chromatin was negative. Cultured leuko cytes showed XY karyotype. At laparotomy, a uterus with normal fallopian tubes was found. An intra-abdominal testis on one side and a streak gonad on the other side were also detected, and confirmed by histologic ...
N, Gadoth, S W, Moses
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Annales de genetique, 1966
THE TERM "mixed gonadal dysgenesis" was first applied in 1964 by Sohval to a condition characterized by ambiguous genitalia with a testis on one side and a rudimentary or absent gonad on the other. Bergada et al1used the term "asymmetrical gonadal dysgenesis" for a similar picture and considered the condition a variant of male pseudohermaphroditism. We
N, Josso +5 more
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THE TERM "mixed gonadal dysgenesis" was first applied in 1964 by Sohval to a condition characterized by ambiguous genitalia with a testis on one side and a rudimentary or absent gonad on the other. Bergada et al1used the term "asymmetrical gonadal dysgenesis" for a similar picture and considered the condition a variant of male pseudohermaphroditism. We
N, Josso +5 more
openaire +4 more sources
Mixed Gonadal Dysgenesis, Pathogensis, and Management
Journal of Pediatric Surgery, 1979Fourteen patients with Mixed Gonadal Dysgenesis who presented as infants or children are discussed. Gonadal asymmetry, and/or sex chromosomal mosaicism, as well as retained Mullerian Ducts characterize the anomaly. The dysgenetic testis may occur as the result of a cascade of development mishaps stemming from abnormalities of H-Y antigen expression or ...
Patricia K. Donahoe +2 more
exaly +3 more sources