Malformations of the central nervous system in trisomy 18 syndrome

Author:

Passarge Eberhard,True Charles W.,Sueoka William T.,Baumgartner Nicholas R.,Keer Kenneth R.

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology and Child Health

Reference49 articles.

1. A 46 chromosome cebocephaly, with remarks on the relation of 13–15 trisomy to holoprosencephaly (arrhinencephaly);DeMyer;Ann. Pediat.,1964

2. Anatomic and histopathologic study of two cases of D1 (13–15) trisomy;Marin-Padilla;Cytogenetics,1964

3. Autosomal abnormalities;Smith;Amer. J. Obst. & Gynec.,1964

4. La trisomie 18. Cinq observations nouvelles. Revue de la littérature;Lafourcade;Ann. Pédiat.,1965

5. Bericht über vier Trisomien 18 und ein Trisomie-18-Mosaik;Wolf;Humangenetik,1965

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1. A review of genetic factors underlying craniorachischisis and omphalocele: Inspired by a unique trisomy 18 case;American Journal of Medical Genetics Part A;2019-06-11

2. Trisomy 18 and Neural Tube Defects;Pediatric Neurology;2013-09

3. The Brain in the 18q- Syndrome;Developmental Medicine & Child Neurology;2008-11-12

4. Neural tube defects and omphalocele in trisomy 18;Clinical Genetics;2008-06-28

5. Chromosomal Abnormalities Associated with Neural Tube Defects (I): Full Aneuploidy;Taiwanese Journal of Obstetrics and Gynecology;2007-12

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