Literature DB >> 3869838

Interstitial deletion of the long arm of chromosome 2: a case report and review of the literature.

Y Takahashi, K Narahara, K Kikkawa, Y Wakita, S Kimura, M Murakami, R Kasai, H Kimoto.   

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Year:  1985        PMID： 3869838     DOI： 10.1007/BF01907967

Source DB:  PubMed          Journal:  Jinrui Idengaku Zasshi        ISSN： 0021-5074


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  3 in total

1.  Probable assignment of soluble isocitrate dehydrogenase (IDH1) to 2q33.3.

Authors:  K Narahara; S Kimura; K Kikkawa; Y Takahashi; Y Wakita; R Kasai; S Nagai; Y Nishibayashi; H Kimoto
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

2.  Hirschsprung disease, microcephaly, mental retardation, and characteristic facial features: delineation of a new syndrome and identification of a locus at chromosome 2q22-q23.

Authors:  D R Mowat; G D Croaker; D T Cass; B A Kerr; J Chaitow; L C Adès; N L Chia; M J Wilson
Journal:  J Med Genet       Date:  1998-08       Impact factor: 6.318

3.  A de novo 10.79 Mb interstitial deletion at 2q13q14.2 involving PAX8 causing hypothyroidism and mullerian agenesis: a novel case report and literature review.

Authors:  Deqiong Ma; Robert Marion; Netra Prasad Punjabi; Elaine Pereira; Joy Samanich; Chhavi Agarwal; Jianli Li; Chih-Kang Huang; K H Ramesh; Linda A Cannizzaro; Rizwan Naeem
Journal:  Mol Cytogenet       Date:  2014-11-26       Impact factor: 2.009
  3 in total

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