SCOPUS 정보 검색 플랫폼

American Journal of Human Genetics

Volumn 59, Issue 4, 1996, Pages 781-792

Molecular definition of the chromosome 7 deletion in Williams syndrome and parent-of-origin effects on growth

(5) Pérez Jurado, Luis A b Peoples, Risa c Kaplan, Paige c Hamel, Ben C J c Francke, Uta a

a STANFORD UNIVERSITY (United States)

b UNIVERSIDAD AUTÓNOMA DE MADRID (Spain)

c NONE

Author keywords

[No Author keywords available]

Indexed keywords

DNA; ELASTIN;

ARTICLE; CHROMOSOME 7Q; CHROMOSOME DELETION; CONTROLLED STUDY; DNA POLYMORPHISM; FEMALE; GENETIC DISTANCE; GENOTYPE; GROWTH RETARDATION; HUMAN; MAJOR CLINICAL STUDY; MALE; MICROCEPHALY; PARENT; PEDIGREE ANALYSIS; PHENOTYPE; PRIORITY JOURNAL; WILLIAMS BEUREN SYNDROME;

ADULT; BLOTTING, SOUTHERN; CHILD; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 7; ELASTIN; GENE DELETION; GENE DOSAGE; GENOMIC IMPRINTING; GENOTYPE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; PEDIGREE; PHENOTYPE; POLYMERASE CHAIN REACTION; POLYMORPHISM, RESTRICTION FRAGMENT LENGTH; WILLIAMS SYNDROME;

EID: 0002391264 PISSN: 00029297 EISSN: None Source Type: Journal
DOI: None Document Type: Article

Times cited : (203)

References (6)

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