Literature DB >> 7083613

Terminal deletion(4)(q33) in a male infant.

J Stamberg, E W Jabs, E Elias.   

Abstract

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Year:  1982        PMID： 7083613     DOI： 10.1111/j.1399-0004.1982.tb00748.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN： 0009-9163            Impact factor:   4.438


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  5 in total

1.  A terminal deletion of the long arm of chromosome 4 [46,XX,del(4)(q33)] in an infant with phenotypic features of Williams syndrome.

Authors:  R D Jefferson; J Burn; K L Gaunt; S Hunter; E V Davison
Journal:  J Med Genet       Date:  1986-10       Impact factor: 6.318

Review 2.  Toward the complete genomic map and molecular pathology of human chromosome 4.

Authors:  O Riess; B Winkelmann; J T Epplen
Journal:  Hum Genet       Date:  1994-07       Impact factor: 4.132

3.  Del(4)(q33----qter): another case report of a child with mild dysmorphism.

Authors:  K A Fagan; R B Morris
Journal:  J Med Genet       Date:  1989-12       Impact factor: 6.318

4.  Molecular definition of a region of chromosome 21 that causes features of the Down syndrome phenotype.

Authors:  J R Korenberg; H Kawashima; S M Pulst; T Ikeuchi; N Ogasawara; K Yamamoto; S A Schonberg; R West; L Allen; E Magenis
Journal:  Am J Hum Genet       Date:  1990-08       Impact factor: 11.025

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
  5 in total

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