4P- SYNDROME - CLINICALLY RECOGNIZABLE CHROMOSOMAL DELETION SYNDROME

被引:61
|
作者
GUTHRIE, RD
AASE, JM
ASPER, AC
SMITH, DW
机构
来源
关键词
D O I
10.1001/archpedi.1971.02110050091011
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
引用
收藏
页码:421 / &
相关论文
共 50 条
  • [1] SHORT ARM DELETION SYNDROME OF CHROMOSOME-4 (4P- SYNDROME)
    ZELLWEGER, H
    BARDACH, J
    BORDWELL, J
    WILLIAMS, K
    [J]. ARCHIVES OF OTOLARYNGOLOGY-HEAD & NECK SURGERY, 1975, 101 (01) : 29 - 32
  • [2] SHORT-ARM DELETION, CHROMOSOME 4, (4P-), A SYNDROME
    TAYLOR, AI
    CHALLACOMBE, DN
    HOWLETT, RM
    [J]. ANNALS OF HUMAN GENETICS, 1970, 34 (OCT) : 137 - +
  • [3] Hand-foot-genital syndrome with a 7p15 deletion: Clinically recognizable syndrome
    Hosoki, Kana
    Ohta, Tohru
    Fujita, Keinosuke
    Nishigaki, Satsuki
    Shiomi, Masashi
    Niikawa, Norio
    Saitoh, Shinji
    [J]. PEDIATRICS INTERNATIONAL, 2012, 54 (03) : e22 - e25
  • [4] OCULAR FINDINGS IN A 4P- DELETION SYNDROME (WOLF-HIRSCHHORN)
    MAYER, UM
    BIALASIEWICZ, AA
    [J]. OPHTHALMIC PAEDIATRICS AND GENETICS, 1989, 10 (01): : 69 - 72
  • [5] DETECTION OF A MOLECULAR DELETION IN A PATIENT WITH THE PHENOTYPE OF THE 4P- SYNDROME BUT NORMAL KARYOTYPE
    SPIEGEL, R
    BINKERT, F
    SCHINZEL, A
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 1991, 49 (04) : 307 - 307
  • [6] OPHTHALMIC FEATURES OF CHROMOSOME DELETION 4P-(WOLF-HIRSCHHORN SYNDROME)
    WILCOX, LM
    BERCOVITCH, L
    HOWARD, RO
    [J]. AMERICAN JOURNAL OF OPHTHALMOLOGY, 1978, 86 (06) : 834 - 839
  • [7] THE ORAL MANIFESTATIONS OF 4P- SYNDROME
    MORISHITA, M
    SHIBA, R
    CHIYO, HA
    FURUYAMA, JI
    FUJITA, H
    ATSUMI, Y
    [J]. JOURNAL OF ORAL AND MAXILLOFACIAL SURGERY, 1983, 41 (09) : 601 - 605
  • [8] OCULAR ANOMALIES AND 4P- SYNDROME
    BATTIN, J
    CHANNAROND, J
    GENAUDEAU, J
    RUFFIE, M
    [J]. JOURNAL DE GENETIQUE HUMAINE, 1976, 24 : 145 - 149
  • [9] 12P TRISOMY - A CLINICALLY RECOGNIZABLE SYNDROME
    HACKEL, E
    COUSINEAU, AJ
    HIGGINS, JV
    KAPUR, S
    PERLOW, R
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 1981, 33 (06) : A105 - A105
  • [10] 3p14p12 deletion syndrome: report of a new case providing further evidence of a clinically recognizable syndrome
    Johnson, Katie
    Yates, Katherine
    Martin, Katherine
    Suri, Mohnish
    [J]. CLINICAL DYSMORPHOLOGY, 2016, 25 (04) : 163 - 166