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- Zhu, Tian
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- Liu, Beihong
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- Wang, Binbin
Producer: 20200615
In:
Journal of medical genetics vol. 56
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Systematic evidence-based review: outcomes from exome and genome sequencing for pediatric patients with congenital anomalies or intellectual disability. [electronic resource] by
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- Hickey, Scott E
- Shen, Jun
Producer: 20210427
In:
Genetics in medicine : official journal of the American College of Medical Genetics vol. 22
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147.
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Whole exome sequencing diagnoses the first fetal case of Bainbridge-Ropers syndrome presenting as pontocerebellar hypoplasia type 1. [electronic resource] by
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- Mechler, Charlotte
- Talhi, Naima
- Martin-Coignard, Dominique
- Roth, Philippe
- Michot, Caroline
- Ichkou, Amale
- Alibeu, Olivier
- Nitschke, Patrick
- Thomas, Sophie
- Vekemans, Michel
- Razavi, Férechté
- Boutaud, Lucile
- Attie-Bitach, Tania
Producer: 20190318
In:
Birth defects research vol. 110
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[Genetic analysis of 10 children with cerebral palsy]. [electronic resource] by
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- Zhang, Lingli
- Lin, Mengsi
- Liu, Jiangyue
- Zhou, Jun
- Sha, Chunxiu
- Zhou, Xiang
Producer: 20190828
In:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics vol. 36
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Multilayer intraclonal heterogeneity in chronic myelomonocytic leukemia. [electronic resource] by
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- Saada, Veronique
- Bilhou-Nabera, Chrystèle
- Hurtado, Ana
- Lordier, Larissa
- Vainchenker, William
- Figueroa, Maria E
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Producer: 20210427
In:
Haematologica vol. 105
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Sequence analysis of 37 candidate genes for male infertility: challenges in variant assessment and validating genes. [electronic resource] by
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Producer: 20210119
In:
Andrology vol. 8
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Infantile hypertrophic pyloric stenosis in patients with esophageal atresia. [electronic resource] by
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- Huigh, Daphne
- van der Helm, Robert M
- Eussen, Bert H F M M
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- IJsselstijn, Hanneke
- Tibboel, Dick
- Wijnen, Rene M H
- de Klein, Annelies
- Hofstra, Robert M W
- Brosens, Erwin
Producer: 20210818
In:
Birth defects research vol. 112
Availability: No items available.
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