Prenatal Detection and Postnatal Follow-Up of Segmental Aneusomies of Chromosome 13 in 4 Consecutive Pregnancies in an Ethnic South Indian Family With a Maternally Inherited Balanced Translocation-Reference-Cited by-同舟云学术

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Prenatal Detection and Postnatal Follow-Up of Segmental Aneusomies of Chromosome 13 in 4 Consecutive Pregnancies in an Ethnic South Indian Family With a Maternally Inherited Balanced Translocation

Published:2015-11-01 Issue:4 Volume:46 Page:343-346
ISSN:0007-5027
Container-title:Laboratory Medicine
language:en
Short-container-title:Lab Med

Author:

Francis Athena,Meleyil Sharrifa Mogaideen,Pullely Jesmi Poulose,Koshy Teena,Batra Meenu Parasuram,Kottukkal Bijoy Balakrishnan,Kannoly Gopinathan Karunakaran

Publisher

Oxford University Press (OUP)

Subject

Biochemistry (medical),Clinical Biochemistry

Link

http://academic.oup.com/labmed/article-pdf/46/4/343/9674277/labmed46-0343.pdf

Reference8 articles.

1. Keify F Zhiyan N Mirzaei F Tootian S Ghazaey S Abbaszadegan MR . Two novel familial balanced translocations t(8;11)(p23;q21) and t(6;16)(q26;p12) implicated in recurrent spontaneous abortion. Arch Iran Med.2012;15:249–252.

2. Barch MJ Knutsen MT Spurbeck JL . The AGT Cytogenetic Laboratory Manual. 3rd Ed. New York: Lippincott Williams & Wilkins; 1997:77–258.

3. Prenatal Diagnosis and Molecular Cytogenetic Characterization of De Novo Partial Trisomy 7p (7p15.3→pter) and Partial Monosomy 13q (13q33.3→qter) Associated With Dandy-Walker Malformation, Abnormal Skull Development and Microcephaly

4. Prenatal diagnosis of 13q- syndrome in a fetus with holoprosencephaly and thumb agenesis

5. Familial translocation with partial trisomy of 13 and 22: evidence that specific regions of chromosomes 13 and 22 are responsible for the phenotype of each trisomy.

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