PLASH - A CANDIDATE GENE FOR KALLMANN SYNDROME AND, MOST LIKELY, A NOVEL ADHESION MOLECULE

被引：0
|
作者：
PETIT, C
机构：
来源：
M S-MEDECINE SCIENCES | 1991年 / 7卷 / 09期
关键词：
D O I：
10.4267/10608/4494
中图分类号：
R-3 [医学研究方法]; R3 [基础医学];
学科分类号：
1001 ;
摘要：
引用
收藏
页码：980 / 980
页数：1
相关论文
共 50 条
  • [21] A novel combination of OHVIRA syndrome and likely causal variant in UMOD gene
    Atraya Samanta
    Syed Monajatur Rahman
    Anil Vasudevan
    Sushmita Banerjee
    CEN Case Reports, 2023, 12 : 249 - 253
  • [22] Exclusion of the β′-COP gene and identification of a novel candidate gene for the blepharophimosis syndrome (BPES).
    De Baere, E
    Roman, E
    Fukushima, Y
    Verhoeven, K
    Van Camp, G
    De Paepe, A
    Messiaen, L
    AMERICAN JOURNAL OF HUMAN GENETICS, 1999, 65 (04) : A224 - A224
  • [23] Identification and Functional Characterization of a Novel Variant in the SEMA3A Gene in a Chinese Family with Kallmann Syndrome
    Shu, Meng
    Wu, Huixiao
    Wei, Shuoshuo
    Shi, Yingzhou
    Li, Zongyue
    Cheng, Yiping
    Fang, Li
    Xu, Chao
    INTERNATIONAL JOURNAL OF ENDOCRINOLOGY, 2022, 2022
  • [24] A case of novel mutation in ANOS1 (KAL1) gene and review of Kallmann syndrome
    Arora, Sumeet
    Yeliosof, Olga
    Chin, Vivian L.
    ENDOCRINOLOGY DIABETES AND METABOLISM CASE REPORTS, 2023, 2023 (02):
  • [25] A novel splice site variant in ANOS1 gene leads to Kallmann syndrome in three siblings
    Jiang, Xiaohui
    Li, Dingming
    Gao, Yanzi
    Zhang, Xueguang
    Wang, Xiang
    Yang, Yihong
    Shen, Ying
    GENE, 2020, 726
  • [26] Identification of a novel mutation in FGFR1 gene in patients with Kallmann syndrome by high throughput sequencing
    Jin, Bao-Fang
    Ji, Zhi-Yong
    Su, Zhi-Ying
    Mei, Li-Bin
    Huang, Xian-Jing
    Lin, Shao-Bin
    Li, Ping
    Sha, Yan-Wei
    SYSTEMS BIOLOGY IN REPRODUCTIVE MEDICINE, 2018, 64 (03) : 202 - 206
  • [27] A novel heterozygous mutation of CHD7 gene in a Chinese patient with Kallmann syndrome: a case report
    Weiwei Xu
    Weibin Zhou
    Haiyang Lin
    Dan Ye
    Guoping Chen
    Fengqin Dong
    Jianguo Shen
    BMC Endocrine Disorders, 21
  • [28] CHARACTERIZATION AND GENE CLONING OF NEUROTACTIN, A NOVEL CELL-ADHESION MOLECULE OF DROSOPHILA
    DELAESCALERA, S
    MARTIN, MD
    JIMENEZ, F
    JOURNAL OF NEUROGENETICS, 1991, 7 (2-3) : 121 - 121
  • [29] Pubertal induction with hCG in a patient with Kallmann syndrome secondary to novel variant in PROK2 gene
    Lucien, Janet N.
    Sadri-Ardekani, Hooman
    Levenson, Amy E.
    HORMONE RESEARCH IN PAEDIATRICS, 2020, 93 : 60 - 61
  • [30] A novel heterozygous mutation of CHD7 gene in a Chinese patient with Kallmann syndrome: a case report
    Xu, Weiwei
    Zhou, Weibin
    Lin, Haiyang
    Ye, Dan
    Chen, Guoping
    Dong, Fengqin
    Shen, Jianguo
    BMC ENDOCRINE DISORDERS, 2021, 21 (01)
12345