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Volumn 110, Issue 1, 2002, Pages 73-77

Terminal deletion of the chromosome 7(q36-qter) in an infant with sacral agenesis and anterior myelomeningocele

Author keywords

Chromosome 7; Chromosome deletion; FISH; Sacral agenesis

Indexed keywords

ARTICLE; CAFE AU LAIT SPOT; CASE REPORT; CHROMOSOME 7Q; CHROMOSOME ANALYSIS; CHROMOSOME DELETION; CHROMOSOME DELETION 7Q; COLOBOMA; FACE MALFORMATION; FLUORESCENCE IN SITU HYBRIDIZATION; GENE LOCATION; HAPLOTYPE; HOMEOBOX; HUMAN; MALE; MENINGOMYELOCELE; MENTAL DEFICIENCY; MICROCEPHALY; PARTIAL MONOSOMY; PRESCHOOL CHILD; PRIORITY JOURNAL; SACRUM AGENESIS;

EID: 0036605109     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.10365     Document Type: Article
Times cited : (24)

References (19)
  • 5
    • 0028233104 scopus 로고
    • Epidemiological analysis of outcomes of pregnancy in diabetic mothers: Identification of the most characteristic and most frequent congenital anomalies
    • (1994) Am J Med Genet , vol.51 , pp. 108-113
    • Martínez-Frías, M.L.1
  • 15
    • 0022531464 scopus 로고
    • Letter to the editor: A further case of cyclopia due to unbalanced segregation of a previously reported rcp(1;7)(q32;q34) familial translocation
    • (1986) Am J Med Genet , vol.24 , pp. 205-206
    • Schinzel, A.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.