A familial interstitial 4q35 deletion with no discernible clinical effects

No abstract is available for this paper.

• Publication year

  2015

• Venue

  American Journal of Medical Genetics. Part A

• Publication date

  2015-08-01

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1002/ajmg.a.37097PMID 25846895
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

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  2014cited by this paper
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  2013cited by this paper
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  2012cited by this paper
• Genotype–phenotype analysis of 4q deletion syndrome: Proposal of a critical region

  2012influential reference
• 4q34.1–q35.2 deletion in a boy with phenotype resembling 22q11.2 deletion syndrome

  2011influential reference
• Identification and molecular characterization of two novel chromosomal deletions associated with autism

  2010cited by this paper
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  2007influential reference
• The tale of a nail sign in chromosome 4q34 deletion syndrome

  2006cited by this paper
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  2006cited by this paper
• A 4q35.2 subtelomeric deletion identified in a screen of patients with co-morbid psychiatric illness and mental retardation

  2004influential reference
• The phenotype of patients with 4q-syndrome.

  2003cited by this paper
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  2002cited by this paper
• The 4q-Syndrome.

  2001cited by this paper
• Interstitial deletion 4q32-34 with ulnar deficiency: 4q33 may be the critical region in 4q terminal deletion syndrome.

  2001cited by this paper
• Child with velocardiofacial syndrome and del (4)(q34.2): another critical region associated with a velocardiofacial syndrome-like phenotype.

  1999influential reference
• Case Report: Two newborns with chromosome 4 imbalances: deletion 4q33 → q35 and ring r (4) (pterq35.2‐qter)

  1997cited by this paper
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  1997cited by this paper
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  1996cited by this paper
• Terminal deletion of the long arm of chromosome 4 in a mother and two sons

  1996influential reference
• Interstitial and terminal deletions of the long arm of chromosome 4: further delineation of phenotypes.

  1988cited by this paper
• 4q- syndrome.

  1979cited by this paper
• A large deletion of the long arm of chromosome No. 4 in a child with limb abnormalities.

  1967cited by this paper

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