TY  - GEN
AU  - Alazami,Anas M
AU  - Al-Qattan,Sarah M
AU  - Faqeih,Eissa
AU  - Alhashem,Amal
AU  - Alshammari,Muneera
AU  - Alzahrani,Fatema
AU  - Al-Dosari,Mohammed S
AU  - Patel,Nisha
AU  - Alsagheir,Afaf
AU  - Binabbas,Bassam
AU  - Alzaidan,Hamad
AU  - Alsiddiky,Abdulmonem
AU  - Alharbi,Nasser
AU  - Alfadhel,Majid
AU  - Kentab,Amal
AU  - Daza,Riza M
AU  - Kircher,Martin
AU  - Shendure,Jay
AU  - Hashem,Mais
AU  - Alshahrani,Saif
AU  - Rahbeeni,Zuhair
AU  - Khalifa,Ola
AU  - Shaheen,Ranad
AU  - Alkuraya,Fowzan S
TI  - Expanding the clinical and genetic heterogeneity of hereditary disorders of connective tissue
SN  - 1432-1203
PY  - 2016///0831
KW  - Amino Acid Sequence
KW  - Cohort Studies
KW  - Connective Tissue Diseases
KW  - genetics
KW  - Exome
KW  - Female
KW  - Genetic Heterogeneity
KW  - Genetic Markers
KW  - High-Throughput Nucleotide Sequencing
KW  - Humans
KW  - Male
KW  - Molecular Sequence Data
KW  - Pedigree
KW  - Phenotype
KW  - Sequence Homology, Amino Acid
KW  - Skin Abnormalities
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1007/s00439-016-1660-z
ER  -