Results
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3881.
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3882.
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Novel HOXA13 mutations and the phenotypic spectrum of hand-foot-genital syndrome. [electronic resource] by
- Goodman, F R
- Bacchelli, C
- Brady, A F
- Brueton, L A
- Fryns, J P
- Mortlock, D P
- Innis, J W
- Holmes, L B
- Donnenfeld, A E
- Feingold, M
- Beemer, F A
- Hennekam, R C
- Scambler, P J
Producer: 20000807
In:
American journal of human genetics vol. 67
Availability: No items available.
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3883.
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3884.
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3885.
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3886.
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3887.
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Early risk factors for neonatal mortality in CAKUT: analysis of 524 affected newborns. [electronic resource] by
- Melo, Batielhe F
- Aguiar, Marcos B
- Bouzada, Maria Candida F
- Aguiar, Regina L
- Pereira, Alamanda K
- Paixão, Gabriela M
- Linhares, Mariana C
- Valerio, Flavia C
- Simões E Silva, Ana Cristina
- Oliveira, Eduardo A
Producer: 20120821
In:
Pediatric nephrology (Berlin, Germany) vol. 27
Availability: No items available.
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3888.
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WNT Signaling Perturbations Underlie the Genetic Heterogeneity of Robinow Syndrome. [electronic resource] by
- White, Janson J
- Mazzeu, Juliana F
- Coban-Akdemir, Zeynep
- Bayram, Yavuz
- Bahrambeigi, Vahid
- Hoischen, Alexander
- van Bon, Bregje W M
- Gezdirici, Alper
- Gulec, Elif Yilmaz
- Ramond, Francis
- Touraine, Renaud
- Thevenon, Julien
- Shinawi, Marwan
- Beaver, Erin
- Heeley, Jennifer
- Hoover-Fong, Julie
- Durmaz, Ceren D
- Karabulut, Halil Gurhan
- Marzioglu-Ozdemir, Ebru
- Cayir, Atilla
- Duz, Mehmet B
- Seven, Mehmet
- Price, Susan
- Ferreira, Barbara Merfort
- Vianna-Morgante, Angela M
- Ellard, Sian
- Parrish, Andrew
- Stals, Karen
- Flores-Daboub, Josue
- Jhangiani, Shalini N
- Gibbs, Richard A
- Brunner, Han G
- Sutton, V Reid
- Lupski, James R
- Carvalho, Claudia M B
Producer: 20181211
In:
American journal of human genetics vol. 102
Availability: No items available.
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3889.
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3890.
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3891.
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3892.
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3893.
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3894.
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3895.
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3896.
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3897.
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3898.
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Cervical length and quantitative fetal fibronectin in the prediction of spontaneous preterm birth in asymptomatic women with congenital uterine anomaly. [electronic resource] by
- Ridout, Alexandra E
- Ibeto, Linda A
- Ross, Georgia N
- Cook, Joanna R
- Sykes, Lynne
- David, Anna L
- Seed, Paul T
- Tribe, Rachel M
- Bennett, Phillip R
- Terzidou, Vasso
- Shennan, Andrew H
- Chandiramani, Manju
- Brown, Richard G
- Chatfield, Susan
- Sadeh, Dana
Producer: 20200311
In:
American journal of obstetrics and gynecology vol. 221
Availability: No items available.
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3899.
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3900.
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Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study. [electronic resource] by
- Ryan, A K
- Goodship, J A
- Wilson, D I
- Philip, N
- Levy, A
- Seidel, H
- Schuffenhauer, S
- Oechsler, H
- Belohradsky, B
- Prieur, M
- Aurias, A
- Raymond, F L
- Clayton-Smith, J
- Hatchwell, E
- McKeown, C
- Beemer, F A
- Dallapiccola, B
- Novelli, G
- Hurst, J A
- Ignatius, J
- Green, A J
- Winter, R M
- Brueton, L
- Brøndum-Nielsen, K
- Scambler, P J
Producer: 19971209
In:
Journal of medical genetics vol. 34
Availability: No items available.
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