Related references
Note: Only part of the references are listed.Private inherited microdeletion/microduplications: Implications in clinical practice
Maria Antonietta Mencarelli et al.
EUROPEAN JOURNAL OF MEDICAL GENETICS (2008)
Bacterial artificial chromosome-emulation oligonucleotide arrays for targeted clinical array-comparative genomic hybridization analyses
Zhishuo Ou et al.
GENETICS IN MEDICINE (2008)
Massively enlarged polycystic kidneys in monozygotic twins with TCF2/HNF-1β (hepatocyte nuclear factor-1β) heterozygous whole-gene deletion
Stanislas Faguer et al.
AMERICAN JOURNAL OF KIDNEY DISEASES (2007)
Recurrent reciprocal genomic Rearrangements of 17q12 are associated with renal disease, diabetes, and epilepsy
Heather C. Mefford et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2007)
LIM-homeodomain proteins Lhx1 and Lhx5, and their cofactor Ldb1, control Purkinje cell differentiation in the developing cerebellum
Yangu Zhao et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2007)
Chromosomal microarray analysis (CMA) detects a large X chromosome deletion including FMR1, FMR2, and IDS in a female patient with mental retardation
Frank J. Probst et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2007)
Clinical Implementation of Chromosomal Microarray Analysis: Summary of 2513 Postnatal Cases
Xinyan Lu et al.
PLOS ONE (2007)
Anomalies of the TCF2 gene are the main cause of fetal bilateral hyperechogenic kidneys
Stephane Decramer et al.
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY (2007)
Renal phenotypes related to hepatocyte nuclear factor-1β (TCF2) mutations in a pediatric cohort
Tim Ulinski et al.
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY (2006)
Genomic disorders: Molecular mechanisms for rearrangements and conveyed phenotypes
JR Lupski et al.
PLOS GENETICS (2005)
Large genomic Rearrangements in the hepatocyte nuclear factor-1β (TCF2) gene are the most frequent cause of maturity-onset diabetes of the young type 5
C Bellanné-Chantelot et al.
DIABETES (2005)
Coordinate roles for LIM homeobox genes in directing the dorsoventral trajectory of motor axons in the vertebrate limb
A Kania et al.
CELL (2000)