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Volumn 8, Issue 2, 1999, Pages 139-141

A de novo deletion of chromosome 15(q15.2q21.2) in a dysmorphic, mentally retarded child with congenital scalp defect

Author keywords

Aplasia cutis congenita; Chromosome 15; High resolution banding; Interstitial deletion

Indexed keywords

ARTICLE; CASE REPORT; CHROMOSOME 15Q; CHROMOSOME BANDING PATTERN; CRANIOFACIAL MALFORMATION; HUMAN; INTERSTITIAL CHROMOSOME DELETION; KARYOTYPING; MALE; METAPHASE CHROMOSOME; PRESCHOOL CHILD; PRIORITY JOURNAL; SCALP; SKIN APLASIA;

EID: 0032929182     PISSN: 09628827     EISSN: None     Source Type: Journal    
DOI: 10.1097/00019605-199904000-00010     Document Type: Article
Times cited : (14)

References (11)
  • 1
    • 0014545047 scopus 로고
    • Scalp defects in trisomy 13
    • Abuelo D, Feingold M (1969). Scalp defects in trisomy 13. Clin Pediatr 8:415-417.
    • (1969) Clin Pediatr , vol.8 , pp. 415-417
    • Abuelo, D.1    Feingold, M.2
  • 2
    • 0023806505 scopus 로고
    • Clinical features in a de novo interstitial deletion 15q13 to q15
    • Autio S, Pihko H, Tengström C (1988). Clinical features in a de novo interstitial deletion 15q13 to q15. Clin Genet 34:293-298.
    • (1988) Clin Genet , vol.34 , pp. 293-298
    • Autio, S.1    Pihko, H.2    Tengström, C.3
  • 3
    • 0029040780 scopus 로고
    • Aplasia cutis congenita and associated disorders: An update
    • Evers M, Steijlen P, Hamel B (1995). Aplasia cutis congenita and associated disorders: an update. Clin Genet 47:295-301.
    • (1995) Clin Genet , vol.47 , pp. 295-301
    • Evers, M.1    Steijlen, P.2    Hamel, B.3
  • 5
    • 0022655534 scopus 로고
    • Aplasia cutis congenita: A clinical review and proposal for classification
    • Frieden IJ (1986). Aplasia cutis congenita: A clinical review and proposal for classification. J. Am Acad Dermatol 14:646-660.
    • (1986) J. Am Acad Dermatol , vol.14 , pp. 646-660
    • Frieden, I.J.1
  • 6
    • 0020043629 scopus 로고
    • Interstitial deletion of the long arm of chromosome 15
    • Fryns J, Muelenaere A, van den Berghe H (1982). Interstitial deletion of the long arm of chromosome 15. Ann Genet 25:59-60.
    • (1982) Ann Genet , vol.25 , pp. 59-60
    • Fryns, J.1    Muelenaere, A.2    Van den Berghe, H.3
  • 7
    • 0025282844 scopus 로고
    • Craniosynostosis in an infant with an interstitial deletion of 15q [46, XY, del (15)(q15q22.1)]
    • Fukushima Y, Wakui K, Nishida T, Nishimoto H (1990). Craniosynostosis in an infant with an interstitial deletion of 15q [46, XY, del (15)(q15q22.1)]. Am J Med Genet 36:209-213.
    • (1990) Am J Med Genet , vol.36 , pp. 209-213
    • Fukushima, Y.1    Wakui, K.2    Nishida, T.3    Nishimoto, H.4
  • 9
    • 0025047781 scopus 로고
    • A de novo interstitial deletion of 15(q21.2q22.1) in a moderately retarded adult male
    • Martin F, Platt J, Tawn E, Burn J (1990). A de novo interstitial deletion of 15(q21.2q22.1) in a moderately retarded adult male. J Med Genet 27:637-639.
    • (1990) J Med Genet , vol.27 , pp. 637-639
    • Martin, F.1    Platt, J.2    Tawn, E.3    Burn, J.4
  • 11
    • 0018168775 scopus 로고
    • The characterization of high-resolution G-banded chromosomes of man
    • Yunis JJ, Sawyer JR, Ball DW (1978). The characterization of high-resolution G-banded chromosomes of man. Chromosoma 67:293-307.
    • (1978) Chromosoma , vol.67 , pp. 293-307
    • Yunis, J.J.1    Sawyer, J.R.2    Ball, D.W.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.