Charcot-Marie-Tooth disease type 1A: the parental origin of a de novo 17p11.2-p12 duplication.
Hertz, J M
Charcot-Marie-Tooth disease type 1A: the parental origin of a de novo 17p11.2-p12 duplication. [electronic resource] - Clinical genetics Oct 1994 - 291-4 p. digital
Publication Type: Journal Article
0009-9163
10.1111/j.1399-0004.1994.tb04162.x doi
Adult
Charcot-Marie-Tooth Disease--genetics
Chromosome Aberrations
Chromosomes, Human, Pair 17
DNA Mutational Analysis
Fathers
Genomic Imprinting
Humans
Male
Pedigree
Repetitive Sequences, Nucleic Acid
Charcot-Marie-Tooth disease type 1A: the parental origin of a de novo 17p11.2-p12 duplication. [electronic resource] - Clinical genetics Oct 1994 - 291-4 p. digital
Publication Type: Journal Article
0009-9163
10.1111/j.1399-0004.1994.tb04162.x doi
Adult
Charcot-Marie-Tooth Disease--genetics
Chromosome Aberrations
Chromosomes, Human, Pair 17
DNA Mutational Analysis
Fathers
Genomic Imprinting
Humans
Male
Pedigree
Repetitive Sequences, Nucleic Acid