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281.
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Ear and hearing problems in relation to karyotype in children with Turner syndrome. [electronic resource] by
- Verver, E J J
- Freriks, K
- Thomeer, H G X M
- Huygen, P L M
- Pennings, R J E
- Alfen-van der Velden, A A E M
- Timmers, H J
- Otten, B J
- Cremers, C W R J
- Kunst, H P M
Producer: 20110914
In:
Hearing research vol. 275
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282.
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283.
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284.
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285.
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Three probands with autistic disorder and isodicentric chromosome 15. [electronic resource] by
- Wolpert, C M
- Menold, M M
- Bass, M P
- Qumsiyeh, M B
- Donnelly, S L
- Ravan, S A
- Vance, J M
- Gilbert, J R
- Abramson, R K
- Wright, H H
- Cuccaro, M L
- Pericak-Vance, M A
Producer: 20000810
In:
American journal of medical genetics vol. 96
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286.
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291.
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292.
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293.
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Loss of TP53 is due to rearrangements involving chromosome region 17p10 approximately p12 in chronic lymphocytic leukemia. [electronic resource] by
- Fink, Stephanie R
- Smoley, Stephanie A
- Stockero, Kimberly J
- Paternoster, Sarah F
- Thorland, Erik C
- Van Dyke, Daniel L
- Shanafelt, Tait D
- Zent, Clive S
- Call, Timothy G
- Kay, Neil E
- Dewald, Gordon W
Producer: 20060724
In:
Cancer genetics and cytogenetics vol. 167
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295.
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Utility of SNP arrays in detecting, quantifying, and determining meiotic origin of tetrasomy 12p in blood from individuals with Pallister-Killian syndrome. [electronic resource] by
- Conlin, Laura K
- Kaur, Maninder
- Izumi, Kosuke
- Campbell, Lindsey
- Wilkens, Alisha
- Clark, Dinah
- Deardorff, Matthew A
- Zackai, Elaine H
- Pallister, Phillip
- Hakonarson, Hakon
- Spinner, Nancy B
- Krantz, Ian D
Producer: 20130807
In:
American journal of medical genetics. Part A vol. 158A
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