Coexistence of Trisomy 13 and SRY (-) XX Ovotesticular Disorder of Sex Development.

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Coexistence of Trisomy 13 and SRY (-) XX Ovotesticular Disorder of Sex Development.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年學術文章

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2017年學術文章

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2017年學術文章

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Coexistence of Trisomy 13 and SRY (-) XX Ovotesticular Disorder of Sex Development.

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Coexistence of Trisomy 13 and SRY

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Coexistence of Trisomy 13 and SRY (-) XX Ovotesticular Disorder of Sex Development.

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Coexistence of Trisomy 13 and SRY

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Coexistence of Trisomy 13 and SRY (-) XX Ovotesticular Disorder of Sex Development.

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Coexistence of Trisomy 13 and SRY

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P1476

Coexistence of Trisomy 13 and SRY (-) XX Ovotesticular Disorder of Sex Development.

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P2093

Gizem Ürel Demir

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Gülen Eda Utine

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Koray Boduroğlu

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Mehmet Alikaşifoğlu

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Pelin Özlem Şimşek Kiper

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Safak Gucer

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Özlem Akgün Doğan

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P2860

Human RSPO1/R-spondin1 is expressed during early ovary development and augments β-catenin signaling

A gene from the human sex-determining region encodes a protein with homology to a conserved DNA-binding motif

SERKAL syndrome: an autosomal-recessive disorder caused by a loss-of-function mutation in WNT4

XX males without SRY gene and with infertility

NR5A1 is a novel disease gene for 46,XX testicular and ovotesticular disorders of sex development

Gene interactions in gonadal development.

Use of probes for ZFY, SRY, and the Y pseudoautosomal boundary in XX males, XX true hermaphrodites, and an XY female.

Autosomal XX sex reversal caused by duplication of SOX9.

46,XX sex reversal.

Multiple synostoses syndrome is due to a missense mutation in exon 2 of FGF9 gene.

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445-451

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scholarly article

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10.1080/15513815.2017.1379039

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P478

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P577

2017-12-08T00:00:00Z

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29220612

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P921

ovotesticular disorder of sex development