Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 10 of 12 for Double Y syndrome
  1. 47,XYY syndrome 
    ... karyotype XYY syndrome YY syndrome Genetic Testing Registry: Double Y syndrome 47,XYY syndrome National Organization for Rare Disorders ( ... extra Y chromosome in males with a 47,XYY karyotype. Hum Mol Genet. 1999 Nov;8(12):2205- ...
    https://medlineplus.gov/genetics/condition/47xyy-syndrome - Genetics
  2. Thanatophoric dysplasia 
    ... V, Legeai-Mallet L. Thanatophoric dysplasia caused by double missense FGFR3 ... DK, Correa A, Vo TM, Wang Y, Hobbs C, Langlois PH, Pearson K, Romitti PA, ...
    https://medlineplus.gov/genetics/condition/thanatophoric-dysplasia - Genetics
  3. Cowden syndrome 
    ... Central Tan MH, Mester J, Peterson C, Yang Y, Chen JL, Rybicki LA, ... syndromes: PTEN-opathies and precision medicine. Endocr Relat Cancer. ...
    https://medlineplus.gov/genetics/condition/cowden-syndrome - Genetics
  4. Subcortical band heterotopia 
    ... cells (germline mutations) usually cause ILS. ... Free article on PubMed Central Ito K, Nakata Y, Matsuda H, Sugai K, Watanabe M, Kamiya K, ...
    https://medlineplus.gov/.../condition/subcortical-band-heterotopia - Genetics
  5. RAPADILINO syndrome 
    ... DNA and temporarily unwind the two spiral strands (double helix) of the DNA molecule. This unwinding ... HA, Sotkasiira J, Biervliet M, Benmansour A, Capri Y, Cormier-Daire V, Crandall B, Hannula-Jouppi K, ...
    https://medlineplus.gov/genetics/condition/rapadilino-syndrome - Genetics
  6. Fish-eye disease 
    ... The molecular basis of lecithin:cholesterol acyltransferase deficiency ... 75 years: a double heterozygote for defined and new mutations affecting LCAT ...
    https://medlineplus.gov/genetics/condition/fish-eye-disease - Genetics
  7. Warsaw breakage syndrome 
    ... DNA and temporarily unwind the two spiral strands (double helix) of the DNA molecule. This ... or Free article on PubMed Central Wu Y, Sommers JA, Khan I, de Winter JP, Brosh ...
    https://medlineplus.gov/genetics/condition/warsaw-breakage-syndrome - Genetics
  8. Baller-Gerold syndrome 
    ... DNA and temporarily unwind the two spiral strands (double helix) of the DNA molecule. This unwinding ... C, Kestila M, Gillerot Y, Megarbane A, Verloes A. Revisiting the craniosynostosis-radial ...
    https://medlineplus.gov/genetics/condition/baller-gerold-syndrome - Genetics
  9. Rothmund-Thomson syndrome 
    ... DNA and temporarily unwind the two spiral strands (double helix) of the DNA molecule. This unwinding is necessary for ... Citation on PubMed Siitonen HA, Sotkasiira J, Biervliet ...
    https://medlineplus.gov/genetics/condition/rothmund-thomson-syndrome - Genetics
  10. 48,XXYY syndrome 
    48,XXYY syndrome is a chromosomal condition that affects development in people who are assigned male at birth. There is a lot of variability in symptoms ...
    https://medlineplus.gov/genetics/condition/48xxyy-syndrome - Genetics
previous · 1 · 2 · next