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2185.
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Cornelia de Lange syndrome: further delineation of phenotype, cohesin biology and educational focus, 5th Biennial Scientific and Educational Symposium abstracts. [electronic resource] by
- Kline, Antonie D
- Calof, Anne L
- Schaaf, Cheri A
- Krantz, Ian D
- Jyonouchi, Soma
- Yokomori, Kyoko
- Gauze, Maria
- Carrico, Cheri S
- Woodman, Julie
- Gerton, Jennifer L
- Vega, Hugo
- Levin, Alex V
- Shirahige, Katsuhiko
- Champion, Michele
- Goodban, Marjorie T
- O'Connor, Julia T
- Pipan, Mary
- Horsfield, Julia
- Deardorff, Matthew A
- Ishman, Stacey L
- Dorsett, Dale
Producer: 20150113
In:
American journal of medical genetics. Part A vol. 164A
Availability: No items available.
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2186.
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Functional paralysis of GM-CSF-derived bone marrow cells productively infected with ectromelia virus. [electronic resource] by
- Szulc-Dąbrowska, Lidia
- Struzik, Justyna
- Ostrowska, Agnieszka
- Guzera, Maciej
- Toka, Felix N
- Bossowska-Nowicka, Magdalena
- Gieryńska, Małgorzata M
- Winnicka, Anna
- Nowak, Zuzanna
- Niemiałtowski, Marek G
Producer: 20170926
In:
PloS one vol. 12
Availability: No items available.
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ROBERTS SYNDROME: CLINICAL AND CYTOGENETIC STUDIES IN 8 EGYPTIAN PATIENTS AND MOLECULAR STUDIES IN 4 PATIENTS WITH GENOTYPE/PHENOTYPE CORRELATION. [electronic resource] by
- Ismail, S
- Essawi, M
- Sedky, N
- Hassan, H
- Fayez, A
- Helmy, N
- Shehab, M
- Farouk, D
- Elruby, M
- Otaify, G
- Eldarsh, A
- Hosny, L
- Gaber, K
- Aboul-Ezz, E H A
- Ramzy, M I
- Mehrez, M I
- Hassib, N F
- Elhadidi, S M A
- Aglan, M S
- Temtamy, S A
Producer: 20181016
In:
Genetic counseling (Geneva, Switzerland) vol. 27
Availability: No items available.
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