![Klinefelter syndrome in males with germ cell tumors: A report from the Children's Oncology Group - Williams - 2018 - Cancer - Wiley Online Library Klinefelter syndrome in males with germ cell tumors: A report from the Children's Oncology Group - Williams - 2018 - Cancer - Wiley Online Library](https://acsjournals.onlinelibrary.wiley.com/cms/asset/1c42b35a-9396-463b-a7d4-9968eb697d2b/cncr31667-fig-0002-m.jpg)
Klinefelter syndrome in males with germ cell tumors: A report from the Children's Oncology Group - Williams - 2018 - Cancer - Wiley Online Library
![Different clinical presentation of Klinefelter's syndrome in monozygotic twins - Benaiges - 2015 - Andrologia - Wiley Online Library Different clinical presentation of Klinefelter's syndrome in monozygotic twins - Benaiges - 2015 - Andrologia - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/ad231917-992a-46a7-b2c6-df96266ef552/and12219-fig-0004-m.jpg)
Different clinical presentation of Klinefelter's syndrome in monozygotic twins - Benaiges - 2015 - Andrologia - Wiley Online Library
![Genetic risk of Klinefelter's syndrome in assisted reproductive technology - Miki - 2017 - Reproductive Medicine and Biology - Wiley Online Library Genetic risk of Klinefelter's syndrome in assisted reproductive technology - Miki - 2017 - Reproductive Medicine and Biology - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/1d8a99a2-5ff1-4c91-903d-25fabf979b75/rmb212029-fig-0001-m.jpg)
Genetic risk of Klinefelter's syndrome in assisted reproductive technology - Miki - 2017 - Reproductive Medicine and Biology - Wiley Online Library
![Boy with 47,XXY,del(15)(q11.2q13) karyotype and Prader–Willi syndrome: A new case and review of the literature - Nowaczyk - 2004 - American Journal of Medical Genetics Part A - Wiley Online Library Boy with 47,XXY,del(15)(q11.2q13) karyotype and Prader–Willi syndrome: A new case and review of the literature - Nowaczyk - 2004 - American Journal of Medical Genetics Part A - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/eef9cf9b-b09a-483c-9c3c-eca3e29bc9e3/mfig001.jpg)
Boy with 47,XXY,del(15)(q11.2q13) karyotype and Prader–Willi syndrome: A new case and review of the literature - Nowaczyk - 2004 - American Journal of Medical Genetics Part A - Wiley Online Library
![Gonadal dysfunction and beyond: Clinical challenges in children, adolescents, and adults with 47,XXY Klinefelter syndrome - Zitzmann - 2020 - American Journal of Medical Genetics Part C: Seminars in Medical Genetics - Wiley Online Library Gonadal dysfunction and beyond: Clinical challenges in children, adolescents, and adults with 47,XXY Klinefelter syndrome - Zitzmann - 2020 - American Journal of Medical Genetics Part C: Seminars in Medical Genetics - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/5d963d37-30c5-4db3-94ec-f0ca41e78aa2/ajmg.v184.2.cover.jpg)
Gonadal dysfunction and beyond: Clinical challenges in children, adolescents, and adults with 47,XXY Klinefelter syndrome - Zitzmann - 2020 - American Journal of Medical Genetics Part C: Seminars in Medical Genetics - Wiley Online Library
![A group of international researchers has uncovered evidence of a super rare genetic condition that gives men an extra X chromosome, reporting the oldest clinical case of Klinefelter Syndrome to date. The A group of international researchers has uncovered evidence of a super rare genetic condition that gives men an extra X chromosome, reporting the oldest clinical case of Klinefelter Syndrome to date. The](https://external-preview.redd.it/dNf7i3-0R60Dg7Bpu-vJCS_MJQyFWydk-KKYMj0Y7gM.jpg?auto=webp&s=5c0860526d3042715e802586c3525557136c1b9f)
A group of international researchers has uncovered evidence of a super rare genetic condition that gives men an extra X chromosome, reporting the oldest clinical case of Klinefelter Syndrome to date. The
![Final Karyotype/Analysis received with true confirmation of XXY however why only 2 cells karyotyped? Trying to determine mosaic or true XXY? Anyone able to help? : r/NIPT Final Karyotype/Analysis received with true confirmation of XXY however why only 2 cells karyotyped? Trying to determine mosaic or true XXY? Anyone able to help? : r/NIPT](https://i.redd.it/1lfd5ka3s9a91.jpg)
Final Karyotype/Analysis received with true confirmation of XXY however why only 2 cells karyotyped? Trying to determine mosaic or true XXY? Anyone able to help? : r/NIPT
![Recognition and management of adults with Turner syndrome: From the transition of adolescence through the senior years - Lin - 2019 - American Journal of Medical Genetics Part A - Wiley Online Library Recognition and management of adults with Turner syndrome: From the transition of adolescence through the senior years - Lin - 2019 - American Journal of Medical Genetics Part A - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/51c0860a-5b3e-4a69-a3e4-d761d334e847/ajmga61310-fig-0004-m.jpg)
Recognition and management of adults with Turner syndrome: From the transition of adolescence through the senior years - Lin - 2019 - American Journal of Medical Genetics Part A - Wiley Online Library
![UPDATE YOUR KNOWLEDGE OF KLINEFELTER SYNDROME | Journal of Psychosocial Nursing and Mental Health Services UPDATE YOUR KNOWLEDGE OF KLINEFELTER SYNDROME | Journal of Psychosocial Nursing and Mental Health Services](https://journals.healio.com/cms/asset/1a56bc49-4fb2-4f49-8596-d1b3302b15be/10.3928_02793695-19850101-05-fig1.jpg)
UPDATE YOUR KNOWLEDGE OF KLINEFELTER SYNDROME | Journal of Psychosocial Nursing and Mental Health Services
![TIL that researchers believe that up to 65% of people with Klinefelter syndrome (XXY chromosomes) are never diagnosed. The condition usually isn't diagnosed until puberty or adulthood because of how mild the TIL that researchers believe that up to 65% of people with Klinefelter syndrome (XXY chromosomes) are never diagnosed. The condition usually isn't diagnosed until puberty or adulthood because of how mild the](https://external-preview.redd.it/til-that-researchers-believe-that-up-to-65-of-people-with-v0-KenA9xqOtNM5Moxp2K6jJuCGn8CDKNrY219ozQSLr4o.jpg?auto=webp&s=7eb20e69eb689ee052693a78645d695f7b7d839d)
TIL that researchers believe that up to 65% of people with Klinefelter syndrome (XXY chromosomes) are never diagnosed. The condition usually isn't diagnosed until puberty or adulthood because of how mild the
![A friend of mine has recently been diagnosed with something called Klinefelters Syndrome. He's rather bravely putting himself out there on the internet to try and raise awareness. I want to try A friend of mine has recently been diagnosed with something called Klinefelters Syndrome. He's rather bravely putting himself out there on the internet to try and raise awareness. I want to try](https://i.ytimg.com/vi/ARlFK1q_EoY/mqdefault.jpg)