Found: 12
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Amniotic fluid biochemistry in isolated polyhydramnios: a series of 464 cases.
- Published in:
- 2015
- By:
- Publication type:
- journal article
Terminal 6q deletions cause brain malformations, a phenotype mimicking heterozygous DLL1 pathogenic variants: A multicenter retrospective case series.
- Published in:
- Prenatal Diagnosis, 2022, v. 42, n. 1, p. 118, doi. 10.1002/pd.6074
- By:
- Publication type:
- Article
Prenatal sonographic patterns in six cases of Wolf-Hirschhorn (4p-) syndrome.
- Published in:
- 2004
- By:
- Publication type:
- journal article
Prenatal Diagnosis of a 'Minor' Form of Brachmann-de Lange Syndrome by Three-Dimensional Sonography and Three-Dimensional Computed Tomography.
- Published in:
- Fetal Diagnosis & Therapy, 2004, v. 19, n. 2, p. 155, doi. 10.1159/000075141
- By:
- Publication type:
- Article
Can a Predetermined Grid and Multidisciplinary Consultation Improve the Description of Cleft lip with or Without Cleft Palate?
- Published in:
- Cleft Palate Craniofacial Journal, 2024, v. 61, n. 7, p. 1143, doi. 10.1177/10556656231156708
- By:
- Publication type:
- Article
Rubinstein‐Taybi Syndrome in a Fetus: Contribution of 2‐ and 3‐Dimensional Ultrasonography.
- Published in:
- 2018
- By:
- Publication type:
- Case Study
Accuracy of Ultrasonography and Magnetic Resonance Imaging in the Diagnosis of Placenta Accreta.
- Published in:
- PLoS ONE, 2014, v. 9, n. 4, p. 1, doi. 10.1371/journal.pone.0094866
- By:
- Publication type:
- Article
Monozygotic triplet pregnancies after single blastocyst transfer: two cases and literature review.
- Published in:
- Reproductive BioMedicine Online (Reproductive Healthcare Limited), 2010, v. 21, n. 3, p. 283, doi. 10.1016/j.rbmo.2010.04.011
- By:
- Publication type:
- Article
Blepharophimosis, short humeri, developmental delay and hirschsprung disease: Expanding the phenotypic spectrum of MED12 mutations.
- Published in:
- American Journal of Medical Genetics. Part A, 2014, v. 164A, n. 7, p. 1821, doi. 10.1002/ajmg.a.36539
- By:
- Publication type:
- Article
Perinatal presentations of non‐immune hydrops fetalis due to recessive PIEZO1 disease: A challenging fetal diagnosis.
- Published in:
- Clinical Genetics, 2023, v. 103, n. 5, p. 560, doi. 10.1111/cge.14274
- By:
- Publication type:
- Article
A Gardos channelopathy associated with nonimmune hydrops and fetal loss.
- Published in:
- Clinical Genetics, 2022, v. 102, n. 6, p. 543, doi. 10.1111/cge.14217
- By:
- Publication type:
- Article
The first two non‐Finnish HYLS1 variants: Expanding the phenotypic spectrum of hydrolethalus syndrome.
- Published in:
- Clinical Genetics, 2021, v. 100, n. 4, p. 462, doi. 10.1111/cge.14021
- By:
- Publication type:
- Article