200 top medical experts on Pallister Killian syndrome across 24 countries and 11 U.S. states, including 21 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.
- Pallister Killian syndrome: Pallister-Killian syndrome (PKS) is a rare multiple congenital anomaly/intellectual deficit syndrome caused by mosaic tissue-limited tetrasomy for chromosome 12p.
- Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
- Support Organizations
- Chromosome Disorder Outreach (CDO)
PO Box 724
Boca Raton, FL 33429
Telephone: +1-561-395-4252
E-mail: https://chromodisorder.org/contact/
Website: https://chromodisorder.org/
- PKS Kids
PO Box 12211
Green Bay, WI 54307
E-mail: gpeters@pkskids.net
Website: http://www.pkskids.net
- Unique – Rare Chromosome Disorder Support Group
G1, The Stables
Station Road West
Surrey
RH8 9EE
United Kingdom
Telephone: +44 (0)1883 723356
E-mail: info@rarechromo.org
Website: https://www.rarechromo.org/
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- Synonyms: Mosaic Hexasomy 12p, Isochromosome 12p syndrome, Pallister-Killian Mosaic Syndrome, Pallister-Killian Syndrome, Teschler-Nicola-Killian Syndrome, mosaic Tetrasomy 12p
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