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Title
Pallister-Killian syndrome
Authors
Keywords
-
Journal
AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS
Volume 166, Issue 4, Pages 406-413
Publisher
Wiley
Online
2014-11-26
DOI
10.1002/ajmg.c.31423
References
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Related references
Note: Only part of the references are listed.- Cardiac manifestations of Pallister-Killian syndrome
- (2014) Richard K. Tilton et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- 12p microRNA expression in fibroblast cell lines from probands with Pallister-Killian syndrome
- (2014) Kosuke Izumi et al. CHROMOSOME RESEARCH
- Genome-Wide Expression Analysis in Fibroblast Cell Lines from Probands with Pallister Killian Syndrome
- (2014) Maninder Kaur et al. PLoS One
- Duplication 12p and Pallister-Killian syndrome: A case report and review of the literature toward defining a Pallister-Killian syndrome minimal critical region
- (2012) Kosuke Izumi et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Seizure characteristics in Pallister-Killian syndrome
- (2012) Meghan S. Candee et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Novel clinical manifestations in Pallister-Killian syndrome: Comprehensive evaluation of 59 affected individuals and review of previously reported cases
- (2012) Alisha Wilkens et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Developmental and behavioral characteristics of individuals with Pallister-Killian syndrome
- (2012) Anna Kostanecka et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Utility of SNP arrays in detecting, quantifying, and determining meiotic origin of tetrasomy 12p in blood from individuals with Pallister-Killian syndrome
- (2012) Laura K. Conlin et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Further evidence for the possible role ofMEIS2in the development of cleft palate and cardiac septum
- (2010) Moira A. Crowley et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Parental origin and mechanisms of formation of three eases of 12p tetrasomy
- (2010) Catherine Turleau et al. CLINICAL GENETICS
- Mosaic tetrasomy 12p
- (2010) S. Gilgenkrantz et al. CLINICAL GENETICS
- Submicroscopic familial chromosomal translocation between 7q and 12p mimicking an autosomal dominant holoprosencephaly syndrome
- (2010) K Izumi et al. CLINICAL GENETICS
- ING4 Mediates Crosstalk between Histone H3 K4 Trimethylation and H3 Acetylation to Attenuate Cellular Transformation
- (2009) Tiffany Hung et al. MOLECULAR CELL
- GATA6 mutations cause human cardiac outflow tract defects by disrupting semaphorin-plexin signaling
- (2009) K. Kodo et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- The ING4 Tumor Suppressor Attenuates NF- B Activity at the Promoters of Target Genes
- (2008) S. Nozell et al. MOLECULAR AND CELLULAR BIOLOGY
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