Pages that link to "Property:P68"
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The following pages link to Canonical URI (P68):
Displaying 50 items.
- Deletions of the short arm of chromosome 6 (Q46883) (← links)
- Deletions of the short arm of chromosome 18 (Q46884) (← links)
- Deletions of chromosome 3 (Q46885) (← links)
- Deletions of the long arm of chromosome 1 (Q46886) (← links)
- Deletions of the short arm of chromosome 3 (Q46887) (← links)
- Deletions of the short arm of chromosome 12 (Q46888) (← links)
- Deletions of chromosome 20 (Q46889) (← links)
- Deletions of chromosome 13 (Q46890) (← links)
- Deletions of chromosome 1 (Q46891) (← links)
- Deletions of the long arm of chromosome 16 (Q46892) (← links)
- Deletions of chromosome 8 (Q46893) (← links)
- Deletions of the short arm of chromosome 8 (Q46894) (← links)
- Deletions of chromosome 15 (Q46895) (← links)
- Deletions of chromosome 14 (Q46896) (← links)
- Deletions of chromosome 17 (Q46897) (← links)
- Deletions of the short arm of chromosome 1 (Q46898) (← links)
- Deletions of chromosome 16 (Q46899) (← links)
- Deletions of the long arm of chromosome 4 (Q46900) (← links)
- Deletions of the long arm of chromosome 17 (Q46901) (← links)
- Deletions of chromosome 12 (Q46902) (← links)
- Deletions of the short arm of chromosome 5 (Q46903) (← links)
- Deletions of chromosome 19 (Q46904) (← links)
- Balanced rearrangements or structural rearrangements (Q46905) (← links)
- Balanced translocation and insertion in normal individual (Q46906) (← links)
- Chromosome inversion in normal individual (Q46907) (← links)
- Balanced autosomal rearrangement in abnormal individual (Q46908) (← links)
- Balanced sex or autosomal rearrangement in abnormal individual (Q46909) (← links)
- Autosomal fragile site (Q46910) (← links)
- Turner syndrome (Q46911) (← links)
- Karyotype 45, X (Q46912) (← links)
- Karyotype 46, X iso Xq (Q46913) (← links)
- Karyotype 46, X with abnormal sex chromosome, except iso Xq (Q46914) (← links)
- Mosaicism, 45, X, 46, XX or XY (Q46915) (← links)
- Mosaicism, 45, X or other cell line with abnormal sex chromosome (Q46916) (← links)
- Karyotype 47,XXX (Q46917) (← links)
- Mosaicism, lines with various numbers of X chromosomes (Q46918) (← links)
- 46,XY gonadal dysgenesis (Q46919) (← links)
- Klinefelter syndrome with karyotype 47,XXY, regular (Q46920) (← links)
- Klinefelter syndrome, male with more than two X chromosomes (Q46921) (← links)
- Klinefelter syndrome (Q46922) (← links)
- Male with double or multiple Y (Q46923) (← links)
- Structural anomalies of chromosome Y (Q46924) (← links)
- Male with sex chromosome mosaicism (Q46925) (← links)
- 46,XX gonadal dysgenesis (Q46926) (← links)
- Early-onset parkinsonism - intellectual deficit (Q46927) (← links)
- Pelizaeus-Merzbacher-like disease (Q46928) (← links)
- Ovotesticular disorder of sex development (Q46929) (← links)
- Androgenetic chimaera (Q46930) (← links)
- Gynogenetic chimaera (Q46931) (← links)
- Chimaera 46, XX, 46, XY (Q46932) (← links)
