Single gene disorders associated with congenital diaphragmatic hernia-Reference-Cited by-同舟云学术

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Single gene disorders associated with congenital diaphragmatic hernia

Published:2007 Issue:2 Volume:145C Page:172-183
ISSN:1552-4868
Container-title:American Journal of Medical Genetics Part C: Seminars in Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Slavotinek Anne M.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference113 articles.

1. A new type of Ehlers-Danlos syndrome associated with tortuous systemic arteries in a large kindred from Qatar

2. Documentation of anomalies not previously described in Fryns syndrome

3. Necrotic gangrenous intrathoracic appendix in a marfanoid adult patient: a case report

4. Congenital diaphragmatic hernia: associated anomalies and antenatal diagnosis

5. Genotype-phenotype correlations of 39 patients with Cornelia De Lange syndrome: the Dutch experience

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1. Hypoxia-Induced Adaptations of Embryonic Fibroblasts: Implications for Developmental Processes;Biology;2024-08-08

2. Role of genetics and the environment in the etiology of congenital diaphragmatic hernia;World Journal of Pediatric Surgery;2024-08

3. Multidisciplinary follow-up in a patient with Morgagni hernia leads to diagnosis of Marfan syndrome;Italian Journal of Pediatrics;2024-05-07

4. Anatomic Disorders of the Chest and Airways;Avery's Diseases of the Newborn;2024

5. Congenital Hepatopulmonary Fusion;European Journal of Pediatric Surgery;2022-08-26

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