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Neurocognitive functioning of a child with partial trisomy 6 and monosomy 21.
Neurocase. 2009;15(2):97-100. doi: 10.1080/13554790802631910. Epub 2009 Jan 26.
3
A young meningitically deaf child with a cochlear implant: a case study.
Int J Pediatr Otorhinolaryngol. 1990 Sep;20(1):25-43. doi: 10.1016/0165-5876(90)90332-l.
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Speech and language development in cognitively delayed children with cochlear implants.
Ear Hear. 2005 Apr;26(2):132-48. doi: 10.1097/00003446-200504000-00003.
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t(15;21)(q15;q22.1) pat resulting in partial trisomy and partial monosomy of chromosomes 15 and 21 in two offspring.
Am J Med Genet. 1996 Dec 2;66(1):45-51. doi: 10.1002/(SICI)1096-8628(19961202)66:1<45::AID-AJMG10>3.0.CO;2-Q.
8
Understanding minds: early cochlear implantation and the development of theory of mind in children with profound hearing impairment.
Int J Pediatr Otorhinolaryngol. 2014 Mar;78(3):537-43. doi: 10.1016/j.ijporl.2013.12.039. Epub 2014 Jan 9.
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The effect of implantation age on visual attention skills.
Int J Pediatr Otorhinolaryngol. 2008 Jun;72(6):869-77. doi: 10.1016/j.ijporl.2008.02.017. Epub 2008 Apr 18.

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Monosomy chromosome 21 compensated by 21q22.11q22.3 duplication in a case with small size and minor anomalies.
Mol Cytogenet. 2018 Aug 1;11:43. doi: 10.1186/s13039-018-0390-4. eCollection 2018.
2
Functional near-infrared spectroscopy for neuroimaging in cochlear implant recipients.
Hear Res. 2016 Aug;338:64-75. doi: 10.1016/j.heares.2016.02.005. Epub 2016 Feb 13.
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Deficiencies in the region syntenic to human 21q22.3 cause cognitive deficits in mice.
Mamm Genome. 2010 Jun;21(5-6):258-67. doi: 10.1007/s00335-010-9262-x. Epub 2010 May 29.

本文引用的文献

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Cognition in children with sensorineural hearing loss: etiologic considerations.
Laryngoscope. 2007 Sep;117(9):1661-5. doi: 10.1097/MLG.0b013e3180ca7834.
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Intelligence, parental depression, and behavior adaptability in deaf children being considered for cochlear implantation.
J Deaf Stud Deaf Educ. 2007 Summer;12(3):335-49. doi: 10.1093/deafed/enm006. Epub 2007 Apr 21.
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Trisomy 6 in basal cell carcinomas correlates with metastatic potential: a dual color fluorescence in situ hybridization study on paraffin sections.
Cancer. 2001 May 15;91(10):1927-32. doi: 10.1002/1097-0142(20010515)91:10<1927::aid-cncr1215>3.0.co;2-r.
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Trisomy 6 is the hallmark of a dysplastic clone in bone marrow aplasia.
Cancer Genet Cytogenet. 1998 Aug;105(1):55-9. doi: 10.1016/s0165-4608(97)00476-7.
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Monosomy 21: a new case confirmed by in situ hybridization.
Hum Genet. 1987 Jan;75(1):95-6. doi: 10.1007/BF00273852.
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A female infant with monosomy 21.
Hum Genet. 1976 Mar 12;31(3):351-3. doi: 10.1007/BF00270866.
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Full monosomy 21: a clinically recognizable syndrome?
Hum Genet. 1977 Jun 30;37(2):155-9. doi: 10.1007/BF00393578.

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