Literature DB >> 3351912

Interstitial deletion (6) (q11----q15) in an infant with congenital abnormalities.

H R Slater1, A Robb, L A Forsyth, D A Hamilton, M C Clark, C A Galloway.   

Abstract

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Mesh：

Year:  1988        PMID： 3351912      PMCID： PMC1015492          DOI： 10.1136/jmg.25.3.210

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


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  3 in total

1.  Congenital anomalies including the VATER association in a patient with del(6)q deletion.

Authors:  R M McNeal; R R Skoglund; U Francke
Journal:  J Pediatr       Date:  1977-12       Impact factor: 4.406

Review 2.  Deletions of the long arm of chromosome 6: two new cases and review of the literature.

Authors:  R S Young; G S Fidone; P A Reider-Garcia; K L Hansen; J L McCombs; C M Moore
Journal:  Am J Med Genet       Date:  1985-01

3.  Interstitial deletion of the long arm of chromosome 6 [del(6) (q16q22)]: case report and review of the literature.

Authors:  M F Schwartz; S Kaffe; S Wallace; R J Desnick
Journal:  Clin Genet       Date:  1984-12       Impact factor: 4.438
  3 in total
  1 in total

1.  Proximal Deletion of 6q Overlapping with Toriello-Carey Facial Phenotype: Prenatal Findings, Clinical Course, Differential Diagnosis, and Review.

Authors:  Sofía Catena; Mariana Aracena; Óscar Pizarro; Karena Espinoza; Guillermo Lay-Son
Journal:  Mol Syndromol       Date:  2017-11-29
  1 in total

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