Results
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9761.
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9762.
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9763.
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9764.
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9765.
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9766.
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9767.
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9768.
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9769.
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9770.
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Mosaicism due to myeloid lineage restricted loss of heterozygosity as cause of spontaneous Rh phenotype splitting. [electronic resource] by
- Körmöczi, Günther F
- Dauber, Eva-Maria
- Haas, Oskar A
- Legler, Tobias J
- Clausen, Frederik B
- Fritsch, Gerhard
- Raderer, Markus
- Buchta, Christoph
- Petzer, Andreas L
- Schönitzer, Diether
- Mayr, Wolfgang R
- Gassner, Christoph
Producer: 20071030
In:
Blood vol. 110
Availability: No items available.
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9771.
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Multiple congenital melanocytic nevi and neurocutaneous melanosis are caused by postzygotic mutations in codon 61 of NRAS. [electronic resource] by
- Kinsler, Veronica A
- Thomas, Anna C
- Ishida, Miho
- Bulstrode, Neil W
- Loughlin, Sam
- Hing, Sandra
- Chalker, Jane
- McKenzie, Kathryn
- Abu-Amero, Sayeda
- Slater, Olga
- Chanudet, Estelle
- Palmer, Rodger
- Morrogh, Deborah
- Stanier, Philip
- Healy, Eugene
- Sebire, Neil J
- Moore, Gudrun E
Producer: 20131031
In:
The Journal of investigative dermatology vol. 133
Availability: No items available.
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9772.
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9773.
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9774.
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9775.
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9776.
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9777.
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9778.
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9779.
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9780.
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Prenatal diagnosis of mosaic ring chromosome 22 associated with cardiovascular abnormalities and intrauterine growth restriction. [electronic resource] by
- Chen, Chih-Ping
- Chern, Schu-Rern
- Chang, Tung-Yao
- Lee, Chen-Chi
- Chen, Li-Feng
- Tzen, Chin-Yuan
- Wang, Wayseen
- Lin, Chen-Ju
- Yang, Brian P T
- Yang, Lawrence S T
Producer: 20030702
In:
Prenatal diagnosis vol. 23
Availability: No items available.
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