Schröer A - Search Results

1

A 1 Mb-sized microdeletion Xq26.2 encompassing the GPC3 gene in a fetus with Simpson-Golabi-Behmel syndrome Report, antenatal findings and review.

Weichert J, Schröer A, Amari F, Siebert R, Caliebe A, Nagel I, Gillessen-Kaesbach G, Mohrmann I, Hellenbroich Y. Weichert J, et al. Among authors: schroer a. Eur J Med Genet. 2011 May-Jun;54(3):343-7. doi: 10.1016/j.ejmg.2011.02.009. Epub 2011 Mar 21. Eur J Med Genet. 2011. PMID: 21362501 Review.

2

Cornelia de Lange syndrome: antenatal diagnosis in two consecutive pregnancies due to rare gonadal mosaicism of NIPBL gene mutation.

Weichert J, Schröer A, Beyer DA, Gillessen-Kaesbach G, Stefanova I. Weichert J, et al. Among authors: schroer a. J Matern Fetal Neonatal Med. 2011 Jul;24(7):978-82. doi: 10.3109/14767058.2010.531312. Epub 2011 Feb 22. J Matern Fetal Neonatal Med. 2011. PMID: 21338332

3

Three- and four-dimensional ultrasound in the diagnosis of fetal tetralogy of fallot with absent pulmonary valve and microdeletion 22q11.

Hartge D, Hoffmann U, Schröer A, Weichert J. Hartge D, et al. Among authors: schroer a. Pediatr Cardiol. 2010 Oct;31(7):1100-3. doi: 10.1007/s00246-010-9748-z. Epub 2010 Jun 16. Pediatr Cardiol. 2010. PMID: 20552182

4

Arthrogryposis multiplex congenita and Pena-Shokeir phenotype: challenge of prenatal diagnosis--report of 21 cases, antenatal findings and review.

Hoellen F, Schröer A, Kelling K, Krapp M, Axt-Fliedner R, Gembruch U, Weichert J. Hoellen F, et al. Among authors: schroer a. Fetal Diagn Ther. 2011;30(4):289-98. doi: 10.1159/000331401. Epub 2011 Dec 8. Fetal Diagn Ther. 2011. PMID: 22156407

5

[Atypical myometric fluid accumulation in graviditate--intramural pregnancy or degenerated fibroid?].

Nause SL, Schröer A, Diedrich K, Weichert J. Nause SL, et al. Among authors: schroer a. Z Geburtshilfe Neonatol. 2012 Oct;216(5):226-9. doi: 10.1055/s-0032-1323792. Epub 2012 Oct 29. Z Geburtshilfe Neonatol. 2012. PMID: 23108967 German.

6

[Congenital gastroschisis--prenatal diagnosis and perinatal management].

Weichert J, Kahl FO, Schröer A, Bohlmann MK, Diedrich K, Hartge DR. Weichert J, et al. Among authors: schroer a. Z Geburtshilfe Neonatol. 2010 Aug;214(4):135-44. doi: 10.1055/s-0030-1255101. Epub 2010 Aug 30. Z Geburtshilfe Neonatol. 2010. PMID: 20806148 Review. German.

7

Novel insights into early embryonic demise via 3D surface rendered imaging in 107 cases.

Hartge DR, Schröer A, Weichert J. Hartge DR, et al. Among authors: schroer a. Ultraschall Med. 2015 Feb;36(1):47-53. doi: 10.1055/s-0033-1350327. Epub 2014 Jan 13. Ultraschall Med. 2015. PMID: 24420719

8

Prenatal imaging and postnatal pathologic work-up in a case of fetal hepatic hamartoma and placental mesenchymal dysplasia.

Ruhland B, Schröer A, Gembruch U, Noack F, Weichert J. Ruhland B, et al. Among authors: schroer a. Ultrasound Obstet Gynecol. 2011 Sep;38(3):360-2. doi: 10.1002/uog.9005. Ultrasound Obstet Gynecol. 2011. PMID: 21432929 Free article. No abstract available.

9

[Foetal rhabdomyosarcoma with massive cardiac and placental infiltration associated with intrauterine foetal death].

Hoellen F, Noack F, Ribbat J, Stefanova I, Schröer A, Bohlmann MK. Hoellen F, et al. Among authors: schroer a. Z Geburtshilfe Neonatol. 2010 Aug;214(4):167-9. doi: 10.1055/s-0030-1261894. Epub 2010 Aug 30. Z Geburtshilfe Neonatol. 2010. PMID: 20806152 German.

10

Trio exome sequencing is highly relevant in prenatal diagnostics.

Gabriel H, Korinth D, Ritthaler M, Schulte B, Battke F, von Kaisenberg C, Wüstemann M, Schulze B, Friedrich-Freksa A, Pfeiffer L, Entezami M, Schröer A, Bürger J, Schwaibold EMC, Lebek H, Biskup S. Gabriel H, et al. Among authors: schroer a. Prenat Diagn. 2022 Jun;42(7):845-851. doi: 10.1002/pd.6081. Epub 2021 Dec 27. Prenat Diagn. 2022. PMID: 34958143 Free PMC article.

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