Genetic analysis of the 15q11-q13 autism candidate region provides continued support for a susceptibility locus

被引：0
|
作者：
Nurmi, EL
Olson, LM
Amin, T
Jacobs, MM
McCauley, JL
Dowd, M
Folstein, SE
Haines, JL
Sutcliffe, JS
机构：
[1] Vanderbilt Univ, Program Human Genet, Nashville, TN USA
[2] Tufts Univ New England Med Ctr, Dept Psychiat, Boston, MA 02111 USA
来源：
AMERICAN JOURNAL OF MEDICAL GENETICS | 2002年 / 114卷 / 07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：
O47
引用
收藏
页码：730 / 730
页数：1
相关论文
共 50 条
  • [21] Genetics of childhood disorders: XLVII. Autism, Part 6: Duplication and inherited susceptibility of chromosome 15q11-q13 genes in autism
    Sutcliffe, JS
    Nurmi, EL
    [J]. JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY, 2003, 42 (02): : 253 - 256
  • [22] Clinical and Genetic Study of a Family With a Paternally Inherited 15q11-q13 Duplication
    Marini, Carla
    Cecconi, Antonella
    Contini, Elisa
    Pantaleo, Marilena
    Metitieri, Tiziana
    Guarducci, Silvia
    Giglio, Sabrina
    Guerrini, Renzo
    Genuardi, Maurizio
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2013, 161A (06) : 1459 - 1464
  • [23] Putative identification of susceptibility genes for autism on 15q11-q13: Role of UBE3A and ATP10A
    Masetti, Guia Guffanti
    Bonati, M. T.
    Gessi, Alessandra
    Cavalleri, Florinda
    Cogliati, Francesca
    Marchi, Margherita
    Lievers, Luisa Strik
    Caffo, Ernesto
    Larizza, Lidia
    Macciardi, Fabio
    Russo, Silvia
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 2006, 141B (07) : 730 - 731
  • [24] Estimate of the prevalence of chromosome 15q11-q13 duplications
    Thomas, NS
    Roberts, SE
    Browne, CE
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2003, 120A (04): : 596 - 598
  • [25] Analysis of a 1-megabase deletion in 15q22-q23 in an autistic patient: Identification of candidate genes for autism and of homologous DNA segments in 15q22-q23 and 15q11-q13
    Smith, M
    Filipek, PA
    Wu, C
    Bocian, M
    Hakim, S
    Modahl, C
    Spence, MA
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 2000, 96 (06): : 765 - 770
  • [26] Prader-Willi syndrome and a deletion/duplication within the 15q11-q13 region
    Butler, MG
    Bittel, D
    Talebizadeh, Z
    [J]. JOURNAL OF MEDICAL GENETICS, 2002, 39 (03) : 202 - 204
  • [27] Mosaic paternal uniparental isodisomy of 15q11-q13 region causing Angelman phenotype
    Narayanan, Dhanya Lakshmi
    Ranganath, Prajnya
    Balakrishnan, Surya
    Dalal, Ashwin
    [J]. CLINICAL DYSMORPHOLOGY, 2019, 28 (04) : 202 - 204
  • [28] Epigenetic Interface of Autism Spectrum Disorders (ASDs): Implications of Chromosome 15q11-q13 Segment
    Mishra, Abhishek
    Prabha, Praisy K.
    Singla, Rubal
    Kaur, Gurjeet
    Sharma, Amit Raj
    Joshi, Rupa
    Suroy, Benjamin
    Medhi, Bikash
    [J]. ACS CHEMICAL NEUROSCIENCE, 2022, 13 (12): : 1684 - 1696
  • [29] CpG island identification and mapping in the autistic disorder region on chromosome 15q11-q13
    Kim, SJ
    Menold, M
    Stajich, J
    Pericak-Vance, MA
    Gilbert, JR
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 2001, 105 (07): : 595 - 595
  • [30] BAC microarray analysis of 15q11-q13 rearrangements and the impact of segmental duplications
    Locke, DP
    Segraves, R
    Nicholls, RD
    Schwartz, S
    Pinkel, D
    Albertson, DG
    Eichler, EE
    [J]. JOURNAL OF MEDICAL GENETICS, 2004, 41 (03) : 175 - 182
12345