TY  - GEN
AU  - Spranger,S
AU  - Schiller,S
AU  - Jauch,A
AU  - Wolff,K
AU  - Rauterberg-Ruland,I
AU  - Hager,D
AU  - Tariverdian,G
AU  - Tröger,J
AU  - Rappold,G
TI  - Léri-Weill syndrome as part of a contiguous gene syndrome at Xp22.3
SN  - 0148-7299
PY  - 1999///0707
KW  - Abnormalities, Multiple
KW  - genetics
KW  - Adult
KW  - Bone and Bones
KW  - abnormalities
KW  - Child, Preschool
KW  - Chromosome Deletion
KW  - Deafness
KW  - Female
KW  - Forearm
KW  - diagnostic imaging
KW  - Homeodomain Proteins
KW  - Humans
KW  - In Situ Hybridization, Fluorescence
KW  - Male
KW  - Mental Disorders
KW  - Radiography
KW  - Seizures
KW  - Sex Chromosome Aberrations
KW  - diagnosis
KW  - Short Stature Homeobox Protein
KW  - Syndrome
KW  - X Chromosome
N1  - Publication Type: Case Reports; Journal Article
UR  - https://doi.org/10.1002/(sici)1096-8628(19990423)83:5<367::aid-ajmg5>3.0.co;2-k
ER  -