Literature DB >> 18688872

Investigation of 4q-deletion in two unrelated patients using array CGH.

S S Kaalund1, R S Møller, A Tészás, M Miranda, G Kosztolanyi, R Ullmann, N Tommerup, Z Tümer.   

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Year:  2008        PMID： 18688872     DOI： 10.1002/ajmg.a.32458

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN： 1552-4825            Impact factor:   2.802


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  7 in total

1.  4q34.1-q35.2 deletion in a boy with phenotype resembling 22q11.2 deletion syndrome.

Authors:  Goran Cuturilo; Björn Menten; Aleksandar Krstic; Danijela Drakulic; Ida Jovanovic; Vojislav Parezanovic; Milena Stevanovic
Journal:  Eur J Pediatr       Date:  2011-07-22       Impact factor: 3.183

2.  Specific inactivation of Twist1 in the mandibular arch neural crest cells affects the development of the ramus and reveals interactions with hand2.

Authors:  Yanping Zhang; Evan L Blackwell; Mitchell T McKnight; Gregory R Knutsen; Wendy T Vu; L Bruno Ruest
Journal:  Dev Dyn       Date:  2012-03-29       Impact factor: 3.780

Review 3.  Clinical and genomic characterization of distal duplications and deletions of chromosome 4q: study of two cases and review of the literature.

Authors:  Michael R Rossi; Miriam S DiMaio; Bixia Xiang; Kangmo Lu; Hande Kaymakcalan; Margretta Seashore; Maurice J Mahoney; Peining Li
Journal:  Am J Med Genet A       Date:  2009-12       Impact factor: 2.802

4.  A familial deletion 4q syndrome: An outcome of a paracentric inversion.

Authors:  Meena Lall; Ratna Puri; Pushpa Saviour; Ishwar Verma
Journal:  Indian J Hum Genet       Date:  2012-05

5.  Novel Vascular Malformation in an Affected Newborn with Deletion Del(4)(q31.3).

Authors:  Norma Elena de León Ojeda; Michel Soriano-Torres; Mercedes J Cabrera; Dunia Bárbara Benítez Ramos
Journal:  Case Rep Genet       Date:  2012-12-25

Review 6.  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.  Prenatal diagnosis of a maternal 7.22-Mb deletion at chromosome 4q32.2q32.3 by SNP array.

Authors:  Pingping Zhang; Yanmei Sun; Ping Huo; Haishen Tian; Jian Gao; Yali Li
Journal:  Mol Cytogenet       Date:  2020-04-10       Impact factor: 2.009
  7 in total

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