… of Pallister–Killian syndrome has been made. Here, we report the clinical findings in 59
individuals with Pallister–Killian syndrome who were ascertained at Pallister–… of Pallister–Killian …

… Pallister first described two institutionalized adult individuals … This syndrome is also
occasionally referred to as Pallister … Pallister first described two institutionalized adult individuals …

… We report the results of a British study into Pallister-Killian … All individuals with Pallister-Killian
syndrome were eligible to … data on 22 patients with Pallister-Killian syndrome. One of the …

* Estimate of the frequency of the malformation or finding in patients with PHS:+++ very
common,++ frequent,+ occasional. The characteristic malformations are in bold type. provide a …

Identification of the isochromosome 12p (i(12p)) associated with Pallister–Killian syndrome
is complicated by the low frequency of this supernumerary chromosome in PHA stimulated …

Pallister‐Killian syndrome is a dysmorphic syndrome characterized by a tissue‐limited
mosaicism: a majority of fibroblasts have 47 chromosomes with an extra small metacentric …

First described in 1977 by Pallister et all and independently reported in 1981 by Killian and
Teschler-Nicola, 2 the syndromeis known for its many anomalies and by various names …

Purpose – This paper is the first of two concerned with a meta‐analysis of the technology
acceptance model (TAM). This part aims to present a narrative literature review of 145 papers …

Pallister‐Killian syndrome (PKS) is a rare sporadic genetic disorder usually caused by
mosaicism of an extra isochromosome of 12p (i(12p)). This retrospective study analysed the …

The first prenatal diagnosis of Pallister-Killian syndrome (PKS) was reported by Gilgenkrantz
et al. in 1985. Since this report, about 60 prenatal cases have been reported but both …