தைஜார்ஜ் நோய்த்தொகை (Tamil Wikipedia)

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Burn, J; Takao, A; Wilson, D; Cross, I; Momma, K; Wadey, R; Scambler, P; Goodship, J (October 1993). "Conotruncal anomaly face syndrome is associated with a deletion within chromosome 22q11.". Journal of Medical Genetics 30 (10): 822–4. doi:10.1136/jmg.30.10.822. பப்மெட்:8230157.

Shprintzen, RJ; Goldberg, RB; Lewin, ML; Sidoti, EJ; Berkman, MD; Argamaso, RV; Young, D (January 1978). "A new syndrome involving cleft palate, cardiac anomalies, typical facies, and learning disabilities: velo-cardio-facial syndrome.". The Cleft palate journal 15 (1): 56–62. பப்மெட்:272242.
Burn, J; Takao, A; Wilson, D; Cross, I; Momma, K; Wadey, R; Scambler, P; Goodship, J (October 1993). "Conotruncal anomaly face syndrome is associated with a deletion within chromosome 22q11.". Journal of Medical Genetics 30 (10): 822–4. doi:10.1136/jmg.30.10.822. பப்மெட்:8230157.

"22q11.2 deletion syndrome". Genetic and Rare Diseases Information Center (GARD) (in ஆங்கிலம்). Archived from the original on 5 July 2017. பார்க்கப்பட்ட நாள் 15 May 2017.

Burn, J; Takao, A; Wilson, D; Cross, I; Momma, K; Wadey, R; Scambler, P; Goodship, J (October 1993). "Conotruncal anomaly face syndrome is associated with a deletion within chromosome 22q11.". Journal of Medical Genetics 30 (10): 822–4. doi:10.1136/jmg.30.10.822. பப்மெட்:8230157.

"22q11.2 deletion syndrome". Genetics Home Reference (in ஆங்கிலம்). July 2013. Archived from the original on 13 May 2017. பார்க்கப்பட்ட நாள் 15 May 2017.

"Chromosome 22q11.2 Deletion Syndrome - NORD (National Organization for Rare Disorders)". NORD (National Organization for Rare Disorders). 2017. Archived from the original on 28 January 2017. பார்க்கப்பட்ட நாள் 10 July 2017.

"22q11.2 deletion syndrome". Genetic and Rare Diseases Information Center (GARD) (in ஆங்கிலம்). Archived from the original on 5 July 2017. பார்க்கப்பட்ட நாள் 15 May 2017.
"Chromosome 22q11.2 Deletion Syndrome - NORD (National Organization for Rare Disorders)". NORD (National Organization for Rare Disorders). 2017. Archived from the original on 28 January 2017. பார்க்கப்பட்ட நாள் 10 July 2017.
"22q11.2 deletion syndrome". Genetics Home Reference (in ஆங்கிலம்). July 2013. Archived from the original on 13 May 2017. பார்க்கப்பட்ட நாள் 15 May 2017.