TY  - GEN
AU  - Spengler,Sabrina
AU  - Begemann,Matthias
AU  - Ortiz Brüchle,Nadina
AU  - Baudis,Michael
AU  - Denecke,Bernd
AU  - Kroisel,Peter Michael
AU  - Oehl-Jaschkowitz,Barbara
AU  - Schulze,Bernd
AU  - Raabe-Meyer,Gisela
AU  - Spaich,Christiane
AU  - Blümel,Peter
AU  - Jauch,Anna
AU  - Moog,Ute
AU  - Zerres,Klaus
AU  - Eggermann,Thomas
TI  - Molecular karyotyping as a relevant diagnostic tool in children with growth retardation with Silver-Russell features
SN  - 1097-6833
PY  - 2013///0110
KW  - Child
KW  - Child, Preschool
KW  - Chromosome Aberrations
KW  - Chromosome Deletion
KW  - Chromosomes, Human, Pair 11
KW  - genetics
KW  - Chromosomes, Human, Pair 7
KW  - Female
KW  - Genetic Markers
KW  - Growth Disorders
KW  - diagnosis
KW  - Humans
KW  - Infant
KW  - Karyotyping
KW  - methods
KW  - Male
KW  - Mutation
KW  - Oligonucleotide Array Sequence Analysis
KW  - Phenotype
KW  - Polymorphism, Single Nucleotide
KW  - Silver-Russell Syndrome
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1016/j.jpeds.2012.04.045
ER  -