Research map: Identification and prenatal diagnosis of a novel likely pathogenic ANOS1 variant in a large Chinese Kallmann syndrome family

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  26. Congenital combined pituitary hormone deficiency patients have better responses to gonadotrophin-induced spermatogenesis than idiopathic hypogonadotropic hypogonadism patients · Jiangfeng Mao · 2015 · 30 citations · Cited by this paper
  27. Expanding the genetic spectrum ofANOS1mutations in patients with congenital hypogonadotropic hypogonadism · Catarina Inês Gonçalves · 2016 · 30 citations · Cited by this paper
  28. Analysis of genetic and clinical characteristics of a Chinese Kallmann syndrome cohort with ANOS1 mutations · Min Nie · 2017 · 24 citations · Cited by this paper
  29. Correlation Analysis of Genotypes and Phenotypes in Chinese Male Pediatric Patients With Congenital Hypogonadotropic Hypogonadism · Yi Wang · 2022 · 14 citations · Cited by this paper
  30. Kallmann syndrome: Diagnostics and management · Rajiv Kumar Yadav · 2024 · 12 citations · Cited by this paper
  31. Kallmann syndrome patient with gender dysphoria, multiple sclerosis, and thrombophilia · Aniruthan Renukanthan · 2015 · 11 citations · Cited by this paper
  32. The KAL1 pVal610Ile mutation is a recessive mutation causing Kallmann syndrome · Shilin Zhang · 2013 · 9 citations · Cited by this paper
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  35. Unilateral renal agenesis as an early marker for genetic screening in Kallmann syndrome · Maria I. Stamou · 2018 · 3 citations · Cited by this paper
  36. ANOS1 variants in a large cohort of Chinese patients with congenital hypogonadotropic hypogonadism. · Zeng Wang · 2022 · 3 citations · Cited by this paper
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