Partial trisomy 9 (9pter->9q22.1) and partial monosomy 14 (14pter>14q11.2) due to paternal translocation t(9;14)(q22.1;q11.2) in a case of Dysmorphic features-Reference-Cited by-同舟云学术

Partial trisomy 9 (9pter->9q22.1) and partial monosomy 14 (14pter>14q11.2) due to paternal translocation t(9;14)(q22.1;q11.2) in a case of Dysmorphic features

Published:2019-02-28 Issue:1 Volume:8 Page:72-77
ISSN:2186-361X
Container-title:Intractable & Rare Diseases Research
language:en
Short-container-title:IRDR

Author:

Dhangar Somprakash¹,Korgaonkar Seema¹,Vundinti Babu Rao¹

Affiliation:

1. National Institute of Immunohaematology (ICMR), K.E.M Hospital campus

Publisher

International Research and Cooperation Association for Bio & Socio-Sciences Advancement (IRCA-BSSA)

Subject

General Medicine

Link

https://www.jstage.jst.go.jp/article/irdr/8/1/8_2019.01000/_pdf

Reference31 articles.

1. 1. Feingold M, Atkins L. A case of trisomy 9. J Med Genet. 1973; 10:184-187.

2. 2. Wilson GN, Raj A, Baker D. The phenotypic and cytogenetic spectrum of partial trisomy 9. Am J Med Genet. 1985; 20:277-282.

3. 3. Yeo L, Waldron R, Lashley S, Day-Salvatore D, Vintzileos AM. Prenatal sonographic findings associated with nonmosaic trisomy 9 and literature review. J Ultrasound Med.2003; 22:425-430.

4. 4. Sepulveda W, Wimalasundera RC, Taylor MJ, Blunt S, Be C, De La Fuente S. Prenatal ultrasound findings in complete trisomy 9. Ultrasound Obstet Gynecol. 2003; 22:479-483.

5. 5. Chitayat D, Hodgkinson K, Luke A, Winsor E, Rose T, Kalousek D. Prenatal diagnosis and fetopathological findings in five fetuses with trisomy 9. Am J Med Genet. 1995; 56:247-251.

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