Results
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142.
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Paternal lineage early onset hereditary ovarian cancers: A Familial Ovarian Cancer Registry study. [electronic resource] by
- Eng, Kevin H
- Szender, J Brian
- Etter, John Lewis
- Kaur, Jasmine
- Poblete, Samantha
- Huang, Ruea-Yea
- Zhu, Qianqian
- Grzesik, Katherine A
- Battaglia, Sebastiano
- Cannioto, Rikki
- Krolewski, John J
- Zsiros, Emese
- Frederick, Peter J
- Lele, Shashikant B
- Moysich, Kirsten B
- Odunsi, Kunle O
Producer: 20180718
In:
PLoS genetics vol. 14
Availability: No items available.
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145.
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146.
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147.
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Parental Origin of Interstitial Duplications at 15q11.2-q13.3 in Schizophrenia and Neurodevelopmental Disorders. [electronic resource] by
- Isles, Anthony R
- Ingason, Andrés
- Lowther, Chelsea
- Walters, James
- Gawlick, Micha
- Stöber, Gerald
- Rees, Elliott
- Martin, Joanna
- Little, Rosie B
- Potter, Harry
- Georgieva, Lyudmila
- Pizzo, Lucilla
- Ozaki, Norio
- Aleksic, Branko
- Kushima, Itaru
- Ikeda, Masashi
- Iwata, Nakao
- Levinson, Douglas F
- Gejman, Pablo V
- Shi, Jianxin
- Sanders, Alan R
- Duan, Jubao
- Willis, Joseph
- Sisodiya, Sanjay
- Costain, Gregory
- Werge, Thomas M
- Degenhardt, Franziska
- Giegling, Ina
- Rujescu, Dan
- Hreidarsson, Stefan J
- Saemundsen, Evald
- Ahn, Joo Wook
- Ogilvie, Caroline
- Girirajan, Santhosh D
- Stefansson, Hreinn
- Stefansson, Kari
- O'Donovan, Michael C
- Owen, Michael J
- Bassett, Anne
- Kirov, George
Producer: 20170512
In:
PLoS genetics vol. 12
Availability: No items available.
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148.
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149.
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Paternal uniparental disomy of chromosome 19 in a pair of monochorionic diamniotic twins with dysmorphic features and developmental delay. [electronic resource] by
- Yeung, Kit San
- Ho, Matthew Sai Pong
- Lee, So Lun
- Kan, Anita Sik Yau
- Chan, Kelvin Yuen Kwong
- Tang, Mary Hoi Yin
- Mak, Christopher Chun Yu
- Leung, Gordon Ka Chun
- So, Po Lam
- Pfundt, Rolph
- Marshall, Christian R
- Scherer, Stephen W
- Choufani, Sanaa
- Weksberg, Rosanna
- Hon-Yin Chung, Brian
Producer: 20191114
In:
Journal of medical genetics vol. 55
Availability: No items available.
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150.
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151.
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A de novo mosaic mutation in SPAST with two novel alternative alleles and chromosomal copy number variant in a boy with spastic paraplegia and autism spectrum disorder. [electronic resource] by
- Matthews, A M
- Tarailo-Graovac, M
- Price, E M
- Blydt-Hansen, I
- Ghani, A
- Drögemöller, B I
- Robinson, W P
- Ross, C J
- Wasserman, W W
- Siden, H
- van Karnebeek, C D
Producer: 20171207
In:
European journal of medical genetics vol. 60
Availability: No items available.
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153.
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154.
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155.
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Dual-spindle formation in zygotes keeps parental genomes apart in early mammalian embryos. [electronic resource] by
- Reichmann, Judith
- Nijmeijer, Bianca
- Hossain, M Julius
- Eguren, Manuel
- Schneider, Isabell
- Politi, Antonio Z
- Roberti, M Julia
- Hufnagel, Lars
- Hiiragi, Takashi
- Ellenberg, Jan
Producer: 20180913
In:
Science (New York, N.Y.) vol. 361
Availability: No items available.
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