DEL(L8P) SYNDROME WITH A SINGLE CENTRAL MAXILLARY INCISOR

被引：0
|
作者：
PERALTA, EM
LANTIGUA, A
机构：
来源：
JOURNAL OF MEDICAL GENETICS | 1994年 / 31卷 / 01期
关键词：
D O I：
暂无
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
引用
收藏
页码：86 / 86
页数：1
相关论文
共 50 条
  • [1] SINGLE MAXILLARY CENTRAL INCISOR IN A GIRL WITH DEL(18P) SYNDROME
    AUGHTON, DJ
    ALSAADI, AA
    TRANSUE, DJ
    JOURNAL OF MEDICAL GENETICS, 1991, 28 (08) : 530 - 532
  • [2] 18P-SYNDROME WITH A SINGLE CENTRAL MAXILLARY INCISOR
    DOLAN, LM
    WILLSON, K
    WILSON, WG
    JOURNAL OF MEDICAL GENETICS, 1981, 18 (05) : 396 - 398
  • [3] The primary maxillary central incisor in the Solitary Median Maxillary Central Incisor syndrome
    Kjaer, I.
    Balslev-Olesen, M.
    EUROPEAN JOURNAL OF PAEDIATRIC DENTISTRY, 2012, 13 (01) : 73 - 75
  • [4] SINGLE CENTRAL MAXILLARY INCISOR AND HOLOPROSENCEPHALY
    HATTORI, H
    OKUNO, T
    MOMOI, T
    KATAOKA, K
    MIKAWA, H
    SHIOTA, K
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1987, 28 (02): : 483 - 487
  • [5] SINGLE CENTRAL MAXILLARY INCISOR AND HOLOPROSENCEPHALY
    FRYNS, JP
    VANDENBERGHE, H
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1988, 30 (04): : 943 - 944
  • [6] SINGLE MEDIAN MAXILLARY CENTRAL INCISOR SYNDROME AND ITS CLINICAL IMPORTANCE
    Aydemir, H.
    Aydemir, S.
    Bezgin, T.
    Ceylaner, S.
    Senel, S.
    GENETIC COUNSELING, 2014, 25 (04): : 453 - 455
  • [7] Eruption of the central incisor, the intermaxillary suture, and maxillary growth in patients with a single median maxillary central incisor
    Becktor, KB
    Sverrild, L
    Pallisgaard, C
    Burhoj, J
    Kjær, I
    ACTA ODONTOLOGICA SCANDINAVICA, 2001, 59 (06) : 361 - 366
  • [8] Solitary maxillary central incisor syndrome: a case report
    Tamayo, Diana Marcela Mamian
    Torres, Richard Fernando Davila
    ODONTOESTOMATOLOGIA, 2022, 24 (40):
  • [9] Solitary median maxillary central incisor (SMMCI) syndrome
    Hall, Roger K.
    ORPHANET JOURNAL OF RARE DISEASES, 2006, 1 (1)
  • [10] Solitary median maxillary central incisor (SMMCI) syndrome
    Roger K Hall
    Orphanet Journal of Rare Diseases, 1
12345