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Volumn 94, Issue 3-4, 2001, Pages 142-146

Molecular and cytogenetic characterisation of a small interstitial de novo 20p13→p12.3 deletion in a patient with severe growth deficit

Author keywords

[No Author keywords available]

Indexed keywords

ALAGILLE SYNDROME; ALLELE; ARTICLE; CASE REPORT; CHROMOSOME 20P; CHROMOSOME BANDING PATTERN; CHROMOSOME DELETION; CLINICAL FEATURE; CYTOGENETICS; DEVELOPMENTAL DISORDER; DISEASE COURSE; FACE DYSMORPHIA; FLUORESCENCE IN SITU HYBRIDIZATION; GROWTH DISORDER; GROWTH RETARDATION; HAPLOTYPE; HUMAN; INFANT; KARYOTYPE; MALE; MOLECULAR GENETICS; MUSCLE HYPOTONIA; PRIORITY JOURNAL;

EID: 0035724442     PISSN: 03010171     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (7)

References (26)
  • 15
    • 0025030040 scopus 로고
    • Partial trisomy 10p in combination with partial monosomy 20p - A syndrome with muscular hypotonia, psychomotor retardation, dwarfism and craniofacial dysmorphia
    • (1990) Klin Padiatr , vol.202 , pp. 352-354
    • Meyer, R.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.