Retrospective evaluation of clinical and molecular data of 148 cases of esophageal atresia-Reference-Cited by-同舟云学术

Retrospective evaluation of clinical and molecular data of 148 cases of esophageal atresia

Published:2022-10-21 Issue:1 Volume:191 Page:77-83
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:American J of Med Genetics Pt A

Author:

Ranza Emmanuelle¹²³^ORCID,Le Gouez Morgane⁴,Guimier Anne¹⁵,Dunlop Naziha Khen⁶,Beaudoin Sylvie⁶,Malan Valérie¹,Michot Caroline¹,Baujat Geneviève¹,Rio Marlène¹,Cormier‐Daire Valérie¹⁵,Abadie Véronique⁴^ORCID,Sarnacki Sabine⁶,Delacourt Christophe⁷,Lyonnet Stanislas¹⁵,Attié‐Bitach Tania¹⁵,Pingault Véronique¹⁵,Rousseau Véronique⁶,Amiel Jeanne¹⁵

Affiliation:

1. Service de médecine génomique des maladies rares Hôpital Necker‐Enfants Malades (AP‐HP centre) Paris France

2. Service de Médecine génétique Hôpitaux Universitaires de Genève Genève Switzerland

3. Medigenome, Swiss Institute of Genomic Medicine Geneva Switzerland

4. Service de Pédiatrie Hôpital Necker‐Enfants Malades (AP‐HP) Paris France

5. Institut Imagine, Inserm U1163, Université de Paris Paris France

6. Service de Chirurgie Viscérale, Urologique et de Transplantation pédiatrique Hôpital Universitaire Necker‐Enfants Malades (AP‐HP et Université de Paris) Paris France

7. Service de Pneumologie Pédiatrique Hôpital Necker‐Enfants Malades (AP‐HP) Paris France

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.a.62989

Reference32 articles.

1. Recurrent constellations of embryonic malformations re‐conceptualized as an overlapping group of disorders with shared pathogenesis

2. Genetic Testing in a Cohort of Complex Esophageal Atresia

3. Bilateral adrenal neuroblastoma and nephroblastoma occurring synchronously in a child with Fanconi's anemia and VACTERL syndrome

4. Clinical and etiological heterogeneity in patients with tracheo-esophageal malformations and associated anomalies

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