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Showing page 1 of results 1 - 9 of about 9 pages

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Mutations in CBX2 Associated with Gonadal Anomalies in 46,XY and 46,XX Individuals | ESPE2019
Tiphanie Merel; Caroline Eozenou; Maldergem Lionel Van; Evgenia Globa; Ken McElreavey; Anu Bashamboo
http://abstracts.eurospe.org/hrp/0092/hrp0092P1-127
Published: 2019-08-22

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Development of Testicular Organoids to Understand Disorders of Sex Development | ESPE2019
Caroline Eozenou; Ken McElreavey; Anu Bashamboo
http://abstracts.eurospe.org/hrp/0092/hrp0092HA1
Published: 2019-08-22

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Mutations in the DEAH-box RNA Helicase DHX37 are a Frequent Cause of 46,XY Gonadal Dysgenesis and 46,XY Testicular Regression Syndrome | ESPE2019
Ken McElreavey; Anne Jorgensen; Caroline Eozenou; Tiphanie Merel; Joelle Bignon-Topalovic; Daisy Tan; Denis Houzelstein; Federic
http://abstracts.eurospe.org/hrp/0092/hrp0092FC10.3
Published: 2019-08-22

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Mutations in CBX2 Associated with Gonadal Anomalies in 46,XY and 46,XX Individuals | ESPE2019
Tiphanie Merel; Caroline Eozenou; Maldergem Lionel Van; Evgenia Globa; Ken McElreavey; Anu Bashamboo
http://abstracts.eurospe.org/hrp/0092/hrp0092p1-127.html
Published: 2019-08-22

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Development of Testicular Organoids to Understand Disorders of Sex Development | ESPE2019
Caroline Eozenou; Ken McElreavey; Anu Bashamboo
http://abstracts.eurospe.org/hrp/0092/hrp0092ha1.html
Published: 2019-08-22

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Mutations in the DEAH-box RNA Helicase DHX37 are a Frequent Cause of 46,XY Gonadal Dysgenesis and 46,XY Testicular Regression Syndrome | ESPE2019
Ken McElreavey; Anne Jorgensen; Caroline Eozenou; Tiphanie Merel; Joelle Bignon-Topalovic; Daisy Tan; Denis Houzelstein; Federic
http://abstracts.eurospe.org/hrp/0092/hrp0092fc10.3.html
Published: 2019-08-22

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A De Novo Missense Mutation in the 4th Zinc Finger of the WT1 Gene Causes 46,XY and 46,XX DSD in Two Sibs | ESPE2018
Rita Bertalan; Balazs Gellen; Caroline Eozenou; Kenneth McElreavey; Anu Bashamboo
http://abstracts.eurospe.org/hrp/0089/hrp0089p1-p222.htm
Published: 2018-08-28

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Mutations Involving Nuclear Receptors and Their Cofactors as a Major Cause of 46,XX DSD | ESPE2018
Anu Bashamboo; Caroline Eozenou; Denis Houzelstein; Joelle Bignon-Topalovic; John Achermann; Ken McElreavey
http://abstracts.eurospe.org/hrp/0089/hrp0089p1-p215.htm
Published: 2018-08-28

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A Mutation in WT1 (Wilms' Tumor Suppressor 1) Associated with 46,XX TDSD | ESPE2016
Caroline Eozenou; Leila Fusee; Ines Mazen; Joelle Bignon-Topalovic; Ken McElreavey; Anu Bashamboo
http://abstracts.eurospe.org/hrp/0086/hrp0086rfc7.4.htm
Published: 2016-08-19

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