Literature DB >> 26348998

Fetal phenotype of 17q12 microdeletion syndrome: renal echogenicity and congenital diaphragmatic hernia in 2 cases.

Patrick Yap1,2, George McGillivray1,2, Fiona Norris1, Joanne M Said2,3,4, Louise Kornman2, Zornitza Stark1,3.   

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Year:  2015        PMID： 26348998     DOI： 10.1002/pd.4690

Source DB:  PubMed          Journal:  Prenat Diagn        ISSN： 0197-3851            Impact factor:   3.050


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  3 in total

Review 1.  The influence of genetics in congenital diaphragmatic hernia.

Authors:  Lan Yu; Rebecca R Hernan; Julia Wynn; Wendy K Chung
Journal:  Semin Perinatol       Date:  2019-08-01       Impact factor: 3.300

2.  Hyperechogenic kidneys and polyhydramnios associated with HNF1B gene mutation.

Authors:  Leire Gondra; Stéphane Décramer; Gihad E Chalouhi; Françoise Muller; Rémi Salomon; Laurence Heidet
Journal:  Pediatr Nephrol       Date:  2016-06-10       Impact factor: 3.714

3.  Phenotypic Variability of 17q12 Microdeletion Syndrome - Three Cases and Review of Literature.

Authors:  A Țuțulan-Cuniță; A G Pavel; L Dimos; M Nedelea; A Ursuleanu; A T Neacșu; M Budișteanu; D Stambouli
Journal:  Balkan J Med Genet       Date:  2022-06-05       Impact factor: 0.810
  3 in total

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