Literature DB >> 4125054

Ring-1 chromosome, microcephalic dwarfism, and acute myeloid leukemia.

M Bobrow, P M Emerson, A I Spriggs, H L Ellis.   

Abstract

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Year:  1973        PMID: 4125054     DOI: 10.1001/archpedi.1973.02110190227024

Source DB:  PubMed          Journal:  Am J Dis Child        ISSN: 0002-922X


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  8 in total

Review 1.  Autosomal ring chromosomes in human genetic disorders.

Authors:  Moh-Ying Yip
Journal:  Transl Pediatr       Date:  2015-04

2.  Clinical consequences of deletion 1p35.

Authors:  S L Wenger; M W Steele; D J Becker
Journal:  J Med Genet       Date:  1988-04       Impact factor: 6.318

Review 3.  Monosomy 1p36.

Authors:  A Slavotinek; L G Shaffer; S K Shapira
Journal:  J Med Genet       Date:  1999-09       Impact factor: 6.318

4.  Letter: Seckel syndrome.

Authors:  G C Szalay
Journal:  J Med Genet       Date:  1974-06       Impact factor: 6.318

5.  Terminal deletion of (1)(q42) and its phenotypical manifestations.

Authors:  M Andrle; A Erlach; W R Mayr; A Rett
Journal:  Hum Genet       Date:  1978-02-23       Impact factor: 4.132

6.  Terminal deletion of the long arm of chromosome 1 in a malformed newborn.

Authors:  E Kessel; R A Pfeiffer; W Blanke; J Schwarz
Journal:  Hum Genet       Date:  1978-06-27       Impact factor: 4.132

Review 7.  The past, present, and future for constitutional ring chromosomes: A report of the international consortium for human ring chromosomes.

Authors:  Peining Li; Barbara Dupont; Qiping Hu; Marco Crimi; Yiping Shen; Igor Lebedev; Thomas Liehr
Journal:  HGG Adv       Date:  2022-09-10

8.  A patient with constitutional ring 1 chromosome characterized by SNP array CGH.

Authors:  Sheila Saliganan; Joanna Lee; Sainan Wei
Journal:  Clin Case Rep       Date:  2016-03-21
  8 in total

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