TY  - GEN
AU  - Liu,W O
AU  - Oefner,P J
AU  - Qian,C
AU  - Odom,R S
AU  - Francke,U
TI  - Denaturing HPLC-identified novel FBN1 mutations, polymorphisms, and sequence variants in Marfan syndrome and related connective tissue disorders
SN  - 1090-6576
PY  - 1999///1012
KW  - Chromatography, High Pressure Liquid
KW  - Connective Tissue Diseases
KW  - diagnosis
KW  - DNA Mutational Analysis
KW  - methods
KW  - Evaluation Studies as Topic
KW  - Exons
KW  - genetics
KW  - Fibrillin-1
KW  - Fibrillins
KW  - Frameshift Mutation
KW  - Genetic Carrier Screening
KW  - Genetic Testing
KW  - Heteroduplex Analysis
KW  - Humans
KW  - Introns
KW  - Marfan Syndrome
KW  - Microfilament Proteins
KW  - Mutation
KW  - Nucleic Acid Hybridization
KW  - Point Mutation
KW  - Polymorphism, Genetic
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S
UR  - https://doi.org/10.1089/gte.1997.1.237
ER  -