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Year | Number of Results |
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1988 | 1 |
1993 | 1 |
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PubMed for Bookshelf ID: 2983900
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Tall stature and minor facial dysmorphisms in a patient with a 17.5 Mb interstitial deletion of chromosome 13 (q14.3q21.33): clinical report and review.
Clin Dysmorphol. 2007 Oct;16(4):279-82. doi: 10.1097/MCD.0b013e3282630818.
Clin Dysmorphol. 2007.
PMID: 17786124
Review.
Molecular investigation of the parental origin of a de novo unbalanced translocation 13/18.
Eggermann T, Engels H, Heidrich-Kaul C, Moderau I, Schwanitz G.
Eggermann T, et al.
Hum Genet. 1997 Apr;99(4):521-2. doi: 10.1007/s004390050399.
Hum Genet. 1997.
PMID: 9099844
Item in Clipboard
Preliminary definition of a "critical region" of chromosome 13 in q32: report of 14 cases with 13q deletions and review of the literature.
Brown S, Gersen S, Anyane-Yeboa K, Warburton D.
Brown S, et al.
Am J Med Genet. 1993 Jan 1;45(1):52-9. doi: 10.1002/ajmg.1320450115.
Am J Med Genet. 1993.
PMID: 8418661
Review.
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Interstitial deletion 13q: further delineation of the syndrome by clinical and high-resolution chromosome analysis of five patients.
Tranebjaerg L, Nielsen KB, Tommerup N, Warburg M, Mikkelsen M.
Tranebjaerg L, et al.
Am J Med Genet. 1988 Apr;29(4):739-53. doi: 10.1002/ajmg.1320290403.
Am J Med Genet. 1988.
PMID: 3400720
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