Pages that link to "Property:P78"
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The following pages link to Knowledge Architect (P78):
Displaying 50 items.
- Oromandibular-limb anomaly syndrome (Q46740) (← links)
- Fronto-otopalatodigital syndromes (Q46741) (← links)
- Ectopic spleen (Q46742) (← links)
- Congenital asplenia (Q46743) (← links)
- Structural developmental anomalies of spleen (Q46744) (← links)
- Polysplenia (Q46745) (← links)
- Congenital adrenal hypoplasia (Q46746) (← links)
- Total mirror imagery (Q46747) (← links)
- Conjoined twins (Q46748) (← links)
- Left isomerism (Q46749) (← links)
- Right isomerism (Q46750) (← links)
- Complete trisomy 21 (Q46751) (← links)
- Maternal imprinting error (Q46753) (← links)
- Duplications of chromosome 22 (Q46755) (← links)
- Duplications of chromosome 12 (Q46757) (← links)
- Duplications of chromosome 2 (Q46759) (← links)
- Duplications of chromosome 16 (Q46761) (← links)
- Duplications of chromosome 19 (Q46763) (← links)
- Duplications of chromosome 5 (Q46765) (← links)
- Duplications of chromosome 10 (Q46767) (← links)
- Duplications of chromosome 13 (Q46769) (← links)
- Male with 46,XX karyotype (Q46771) (← links)
- Uniparental disomies of maternal origin (Q46773) (← links)
- Number anomalies of chromosome X (Q46775) (← links)
- Duplications of chromosome 6 (Q46777) (← links)
- Uniparental disomies of paternal origin (Q46779) (← links)
- Duplications of chromosome 20 (Q46781) (← links)
- Structural anomalies of chromosome X, excluding Turner syndrome (Q46783) (← links)
- Uniparental disomies (Q46785) (← links)
- Duplications of chromosome 3 (Q46786) (← links)
- Duplications of chromosome 1 (Q46787) (← links)
- Duplications of chromosome 9 (Q46788) (← links)
- Duplications of chromosome 18 (Q46789) (← links)
- Duplications of chromosome 15 (Q46790) (← links)
- Duplications of chromosome 14 (Q46791) (← links)
- Duplications of chromosome 4 (Q46792) (← links)
- Paternal imprinting error (Q46793) (← links)
- Duplications of the autosomes (Q46794) (← links)
- Imprinting errors (Q46795) (← links)
- Extra ring or dicentric chromosomes (Q46796) (← links)
- Duplications of chromosome 11 (Q46797) (← links)
- Duplications of chromosome 21 (Q46798) (← links)
- Duplications of chromosome 7 (Q46799) (← links)
- Duplications of chromosome 17 (Q46800) (← links)
- Complete trisomies of the autosomes (Q46801) (← links)
- Number anomalies of chromosome Y (Q46802) (← links)
- Duplications of chromosome 8 (Q46803) (← links)
- Complete monosomies of the autosomes (Q46804) (← links)
- Complete trisomy 13 (Q46805) (← links)
- Complete trisomy 18 (Q46806) (← links)
