|
|
|
Volumn 74, Issue 219, 1996, Pages 33-36
|
|
Prenatal diagnosis of choroideremia
a
|
|
Author keywords
Choroideremia; Mutation; Prenatal diagnosis; RFLP
|
|
Indexed keywords
ARTICLE;
BLINDNESS;
CHOROIDEREMIA;
CLINICAL ARTICLE;
FETUS;
GENE LOCUS;
GENE MAPPING;
GENE MUTATION;
GENETIC COUNSELING;
GENETIC LINKAGE;
HUMAN;
MALE;
MOLECULAR CLONING;
PRENATAL DIAGNOSIS;
PRIORITY JOURNAL;
RESTRICTION FRAGMENT LENGTH POLYMORPHISM;
X CHROMOSOME LINKED DISORDER;
ADULT;
CASE REPORT;
FEMALE;
GENETICS;
MOLECULAR GENETICS;
MUTATION;
NUCLEOTIDE SEQUENCE;
PEDIGREE;
PREGNANCY;
SEX CHROMOSOME ABERRATION;
X CHROMOSOME;
DNA;
ADULT;
BASE SEQUENCE;
CHOROIDEREMIA;
DNA;
FEMALE;
HUMANS;
LINKAGE (GENETICS);
MALE;
MOLECULAR SEQUENCE DATA;
MUTATION;
PEDIGREE;
POLYMORPHISM, RESTRICTION FRAGMENT LENGTH;
PREGNANCY;
PRENATAL DIAGNOSIS;
SEX CHROMOSOME ABERRATIONS;
X CHROMOSOME;
|
|
EID: 0029665992
PISSN: 13953931
EISSN: None
Source Type: Journal
DOI: None Document Type: Article |
|
Times cited : (8)
|
|
References (0)
|
