Literature DB >> 9378903

Deletion (4)(q33 --> qter): a case report and review of the literature.

Z Borochowitz1, S A Shalev, I Yehudai, H Bar-el, H Dar, E Tirosh.   

Abstract

Mesh：

Year:  1997        PMID： 9378903     DOI： 10.1177/088307389701200510

Source DB:  PubMed          Journal:  J Child Neurol        ISSN： 0883-0738            Impact factor:   1.987


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  7 in total

Review 1.  Hand factors as regulators of cardiac morphogenesis and implications for congenital heart defects.

Authors:  Joshua W Vincentz; Ralston M Barnes; Anthony B Firulli
Journal:  Birth Defects Res A Clin Mol Teratol       Date:  2011-04-01

2.  Hand2 elevates cardiomyocyte production during zebrafish heart development and regeneration.

Authors:  Yocheved L Schindler; Kristina M Garske; Jinhu Wang; Beth A Firulli; Anthony B Firulli; Kenneth D Poss; Deborah Yelon
Journal:  Development       Date:  2014-07-18       Impact factor: 6.868

3.  Terminal 4q deletion syndrome.

Authors:  C M Kuldeep; A K Khare; Anubhav Garg; Asit Mittal; Lalit Gupta
Journal:  Indian J Dermatol       Date:  2012-05       Impact factor: 1.494

4.  HAND transcription factors cooperatively specify the aorta and pulmonary trunk.

Authors:  Joshua W Vincentz; Beth A Firulli; Kevin P Toolan; Marco Osterwalder; Len A Pennacchio; Anthony B Firulli
Journal:  Dev Biol       Date:  2021-03-20       Impact factor: 3.148

5.  Investigation of Chromosomal Abnormalities and Microdeletion/ Microduplication(s) in Fifty Iranian Patients with Multiple Congenital Anomalies.

Authors:  Akbar Mohammadzadeh; Susan Akbaroghli; Ehsan Aghaei-Moghadam; Nejat Mahdieh; Reza Shervin Badv; Payman Jamali; Roxana Kariminejad; Zahra Chavoshzadeh; Saghar Ghasemi Firouzabadi; Roxana Mansour Ghanaie; Ahoura Nozari; Sussan Banihashemi; Fatemeh Hadipour; Zahra Hadipour; Ariana Kariminejad; Hossein Najmabadi; Yousef Shafeghati; Farkhondeh Behjati
Journal:  Cell J       Date:  2019-06-15       Impact factor: 2.479

6.  Different Cardiac Anomalies in Mother and Son with 4q-Syndrome.

Authors:  Marcello Marcì; Angela Guarina; M Cristina Castiglione; Nicola Sanfilippo
Journal:  Case Rep Genet       Date:  2015-08-31

Review 7.  Terminal chromosome 4q deletion syndrome in an infant with hearing impairment and moderate syndromic features: review of literature.

Authors:  Barbara Vona; Indrajit Nanda; Cordula Neuner; Jörg Schröder; Vera M Kalscheuer; Wafaa Shehata-Dieler; Thomas Haaf
Journal:  BMC Med Genet       Date:  2014-06-25       Impact factor: 2.103
  7 in total

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