TY  - GEN
AU  - Fernández,Raquel M
AU  - Sánchez,Javier
AU  - García-Díaz,Lutgardo
AU  - Peláez-Nora,Yolanda
AU  - González-Meneses,Antonio
AU  - Antiñolo,Guillermo
AU  - Borrego,Salud
TI  - Interstitial 10p deletion derived from a maternal ins(16;10)(q22;p13p15.2): Report of the first familial case of 10p monosomy affecting to two familial members of different generations
SN  - 1552-4833
PY  - 2017///0104
KW  - Adult
KW  - Child
KW  - Chromosome Deletion
KW  - Chromosome Disorders
KW  - genetics
KW  - Chromosomes, Human, Pair 10
KW  - Comparative Genomic Hybridization
KW  - Developmental Disabilities
KW  - DiGeorge Syndrome
KW  - Gene Deletion
KW  - Hearing Loss, Sensorineural
KW  - Humans
KW  - Hypoparathyroidism
KW  - In Situ Hybridization, Fluorescence
KW  - Karyotyping
KW  - Male
KW  - Nephrosis
N1  - Publication Type: Case Reports; Journal Article
UR  - https://doi.org/10.1002/ajmg.a.37559
ER  -