相关参考文献
注意：仅列出部分参考文献，下载原文获取全部文献信息。P57(KIP2) immunostaining and molecular cytogenetics: combined approach aids in diagnosis of morphologically challenging cases with molar phenotype and in detecting androgenetic cell tines in mosaic/chimeric conceptions
Lori Hoffner et al.
HUMAN PATHOLOGY (2008)
Hepatic mesenchymal hamartoma: A disorder of imprinting?
Robyn C. Reed et al.
PEDIATRIC AND DEVELOPMENTAL PATHOLOGY (2008)
Utility of microsatellite analysis in evaluation of pregnancies with placental mesenchymal dysplasia
Marie N. Schuetzle et al.
PRENATAL DIAGNOSIS (2007)
Mesenchymal hamartoma of the liver associated with features of Beckwith-Wiedemann Syndrome and high serum alpha-fetoprotein levels
Mariana M. Cajaiba et al.
PEDIATRIC AND DEVELOPMENTAL PATHOLOGY (2007)
Origin and outcome of pregnancies affected by androgenetic/biparental chimerism
Wendy P. Robinson et al.
HUMAN REPRODUCTION (2007)
Molecular diagnosis of Beckwith-Wiedemann Syndrome using quantitative methylation-sensitive polymerase chain reaction
Bradford Coffee et al.
GENETICS IN MEDICINE (2006)
Placental mesenchymal dysplasia is associated with high rates of intrauterine growth restriction and fetal demise - A report of 11 new cases and a review of the literature
T Pham et al.
AMERICAN JOURNAL OF CLINICAL PATHOLOGY (2006)
Congenital hyperinsulinism and mosaic abnormalities of the ploidy
I Giurgea et al.
JOURNAL OF MEDICAL GENETICS (2006)
Androgenetic/biparental mosaicism causes placental mesenchymal dysplasia
KA Kaiser-Rogers et al.
JOURNAL OF MEDICAL GENETICS (2006)
p57(KIP2) immunostaining in the diagnosis of complete versus partial hydatidiform moles
NJ Sebire et al.
HISTOPATHOLOGY (2006)
Differential diagnosis between complete and partial mole by TSSC3 antibody completely correlates to DNA diagnosis
H Kato et al.
DIAGNOSTIC MOLECULAR PATHOLOGY (2005)
Beckwith-Wiedemann syndrome: Historical, clinicopathological, and etiopathogenetic perspectives
MM Cohen
PEDIATRIC AND DEVELOPMENTAL PATHOLOGY (2005)
Hepatic mesenchymal hamartoma with translocation involving chromosome band 19q13.4: a recurrent abnormality
D Rakheja et al.
CANCER GENETICS AND CYTOGENETICS (2004)
The product of the imprinted gene IPL marks human villous cytotrophoblast and is lost in complete hydatidiform mole
A Saxena et al.
PLACENTA (2003)
The maternally transcribed gene p57KIP2 (CDNK1C) is abnormally expressed in both androgenetic and biparental complete hydatidiform moles
RA Fisher et al.
HUMAN MOLECULAR GENETICS (2002)
Discrimination of complete hydatidiform mole from its mimics by immunohistochemistry of the paternally imprinted gene product p57KIP2
DH Castrillon et al.
AMERICAN JOURNAL OF SURGICAL PATHOLOGY (2001)
Tumour suppressor activity of human imprinted gene PEG3 in a glioma cell line
T Kohda et al.
GENES TO CELLS (2001)
Mesenchymal hamartoma of the liver in Beckwith-Wiedemann syndrome:: The first reported case
JP García-de-la-Torre et al.
PEDIATRIC PATHOLOGY & MOLECULAR MEDICINE (2000)
分享论文
