Prenatal diagnosis of charcot‐marie‐tooth disease type 1a (CMT1A) using molecular genetic techniques

Prenatal Diagnosis

Volumn 15, Issue 7, 1995, Pages 633-640

  Navon, R ^a   Timmerman, V ^b   Lofgren A ^b   Liang, P ^b   Nelis, E ^b   Zeitune, M ^c,d   Van Broeckhoven, C ^b  

^a TEL AVIV UNIVERSITY   (Israel)

^b UNIVERSITY OF ANTWERP   (Belgium)

^c Genetic Clinic ^*  (Israel)

^d MEIR MEDICAL CENTER   (Israel)

Author keywords

Charcot Marie Tooth disease; CMT1A; duplication 17p11.2; motor and sensory neuropathy; type 1A

Indexed keywords

REPETITIVE DNA;

ARTICLE; CASE REPORT; FETUS; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; MALE; MOLECULAR GENETICS; NUCLEOTIDE REPEAT; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; TANDEM REPEAT;

ADULT; BASE SEQUENCE; BLOTTING, SOUTHERN; CASE REPORT; CHARCOT-MARIE-TOOTH DISEASE; DNA; FEMALE; HUMAN; KARYOTYPING; MALE; MOLECULAR BIOLOGY; MOLECULAR SEQUENCE DATA; NEURAL CONDUCTION; PEDIGREE; POLYMORPHISM, RESTRICTION FRAGMENT LENGTH; PREGNANCY; PRENATAL DIAGNOSIS; REPETITIVE SEQUENCES, NUCLEIC ACID; SUPPORT, NON-U.S. GOV'T;

EID: 0029007808     PISSN: 01973851     EISSN: 10970223     Source Type: Journal    
DOI: 10.1002/pd.1970150708     Document Type: Article

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