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Results 1 - 9 of 9 for Anomaly of sex chromosome
  1. 48,XXYY syndrome 
    ... 48,XXYY embryo. XXYY syndrome Genetic Testing Registry: Anomaly of sex chromosome 48,XXYY syndrome National Organization for Rare Disorders ( ...
    https://medlineplus.gov/genetics/condition/48xxyy-syndrome - Genetics
  2. 49,XXXXY syndrome 
    ... have learned more about the differences between these sex chromosome disorders, they have started to ... Genetic ...
    https://medlineplus.gov/genetics/condition/49xxxxy-syndrome - Genetics
  3. Trisomy 18 
    ... Edwards syndrome phenotype to two noncontiguous regions on chromosome 18. Am J ... and associated major anomalies among fetal trisomy 18 cases with different cell ...
    https://medlineplus.gov/genetics/condition/trisomy-18 - Genetics
  4. Microphthalmia with linear skin defects syndrome 
    ... X chromosome, which is one of the two sex chromosomes. In females (who have two X ... defects syndrome National ...
    https://medlineplus.gov/...thalmia-with-linear-skin-defects-syndrome - Genetics
  5. Turner syndrome 
    ... only one copy of the X chromosome. Other sex chromosome abnormalities are also possible in people with ... CA. Major vascular anomalies in Turner syndrome: prevalence and magnetic resonance angiographic ...
    https://medlineplus.gov/genetics/condition/turner-syndrome - Genetics
  6. FG syndrome 
    ... X chromosome, which is one of the two sex chromosomes. In males (who have only one X chromosome), one ... an X-linked multiple congenital anomaly syndrome: the clinical phenotype and an algorithm for ...
    https://medlineplus.gov/genetics/condition/fg-syndrome - Genetics
  7. X-linked chondrodysplasia punctata 2 
    ... X chromosome, which is one of the two sex chromosomes. In females (who have two X chromosomes), ... AF. A novel X-linked multiple congenital anomaly syndrome associated with an EBP mutation. Am J ...
    https://medlineplus.gov/.../x-linked-chondrodysplasia-punctata-2 - Genetics
  8. Aicardi syndrome 
    ... whether a person will develop male or female sex characteristics. Genes on these ... syndrome Aicardi ...
    https://medlineplus.gov/genetics/condition/aicardi-syndrome - Genetics
  9. Léri-Weill dyschondrosteosis 
    ... on either the X chromosome or the Y chromosome.A related skeletal disorder called Langer ... of 22 children with SHOX anomalies and familial short stature suggestive of Leri-Weill ...
    https://medlineplus.gov/.../condition/leri-weill-dyschondrosteosis - Genetics