Literature DB >> 21371014

Chromosome 8p23.2-pter: a critical region for mental retardation, autism and epilepsy?

A Nucaro, T Pisano, I Chillotti, C Montaldo, D Pruna.   

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Year:  2011        PMID: 21371014     DOI: 10.1111/j.1399-0004.2010.01548.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


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  6 in total

1.  The de novo aberration rate of prenatal karyotype was comparable between 1496 fetuses conceived via IVF/ICSI and 1396 fetuses from natural conception.

Authors:  Shimin Yuan; Liuliang Guo; Dehua Cheng; Xiurong Li; Hao Hu; Liang Hu; Guangxiu Lu; Ge Lin; Fei Gong; Yue-Qiu Tan
Journal:  J Assist Reprod Genet       Date:  2022-05-26       Impact factor: 3.357

2.  Neuroimaging Features of San Luis Valley Syndrome.

Authors:  Matthew T Whitehead; Bonmyong Lee
Journal:  Case Rep Radiol       Date:  2015-09-06

3.  Copy number variations in Saudi family with intellectual disability and epilepsy.

Authors:  Muhammad I Naseer; Adeel G Chaudhary; Mahmood Rasool; Gauthaman Kalamegam; Fai T Ashgan; Mourad Assidi; Farid Ahmed; Shakeel A Ansari; Syed Kashif Zaidi; Mohammed M Jan; Mohammad H Al-Qahtani
Journal:  BMC Genomics       Date:  2016-10-17       Impact factor: 3.969

4.  Chromosomal Microarray Analysis in Turkish Patients with Unexplained Developmental Delay and Intellectual Developmental Disorders.

Authors:  Hakan Gürkan; Emine İkbal Atli; Engin Atli; Leyla Bozatli; Mengühan Araz Altay; Sinem Yalçintepe; Yasemin Özen; Damla Eker; Çisem Akurut; Selma Demır; Işık Görker
Journal:  Noro Psikiyatr Ars       Date:  2020-05-05       Impact factor: 1.339

5.  Isolated chromosome 8p23.2‑pter deletion: Novel evidence for developmental delay, intellectual disability, microcephaly and neurobehavioral disorders.

Authors:  Shanshan Shi; Shaobin Lin; Baojiang Chen; Yi Zhou
Journal:  Mol Med Rep       Date:  2017-09-07       Impact factor: 2.952

6.  Clinical Manifestations of Various Molecular Cytogenetic Variants of Eight Cases of "8p Inverted Duplication/Deletion Syndrome".

Authors:  Darya A Yurchenko; Marina E Minzhenkova; Elena L Dadali; Zhanna G Markova; Galina E Rudenskaya; Galina N Matyushchenko; Ilya V Kanivets; Nadezda V Shilova
Journal:  Biomedicines       Date:  2022-02-28
  6 in total

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