<i>FGF9</i> variant in 46, <scp>XY DSD</scp> patient suggests a role for dimerization in sex determination-Reference-Cited by-同舟云学术

FGF9 variant in 46, XY DSD patient suggests a role for dimerization in sex determination

Published:2022-11-28 Issue:3 Volume:103 Page:277-287
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clinical Genetics

Author:

Croft Brittany¹²³,Bird Anthony D.¹²,Ono Makoto¹⁴^ORCID,Eggers Stefanie³,Bagheri‐Fam Stefan¹²,Ryan Janelle M.¹,Reyes Alejandra P.¹,van den Bergen Jocelyn³,Baxendale Anne⁴⁵,Thompson Elizabeth M.⁵⁶,Kueh Andrew J.⁷,Stanton Peter¹²,Thomas Tim⁷^ORCID,Sinclair Andrew H.³⁸^ORCID,Harley Vincent R.²

Affiliation:

1. Hudson Institute of Medical Research Monash Medical Centre Melbourne Australia

2. Department of Molecular & Translational Science Monash University Melbourne Australia

3. Murdoch Children's Research Institute Melbourne Australia

4. Department of Paediatrics Chiba Kaihin Municipal Hospital Chiba Japan

5. SA Clinical Genetics Service Women's and Children's Hospital Adelaide Australia

6. Adelaide Medical School, Faculty of Health Sciences University of Adelaide Adelaide Australia

7. The Walter and Eliza Hall Institute of Medical Research, Parkville Melbourne Australia

8. Department of Paediatrics University of Melbourne Melbourne Australia

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/cge.14261

Reference44 articles.

1. Consensus statement on management of intersex disorders

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3. New insights from unbiased panel and whole-exome sequencing in a large Chinese cohort with disorders of sex development

4. Building the mammalian testis: origins, differentiation, and assembly of the component cell populations

5. Testis Determination Requires a Specific FGFR2 Isoform to Repress FOXL2

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