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Kleeblattschadel anomaly and partial trisomy for chromosome 13 (47,XY,+der(13),t(3,13)(q24;

  • Published:2008-04-23 Issue:6 Volume:17 Page:409-414
  • ISSN:0009-9163
  • Container-title:Clinical Genetics
  • language:en
  • Short-container-title:

Author:

McCorquodale M.,Erickson R. P.,Robinson M.,Roszczipka K.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference20 articles.

1. Localization of genes on chromosome 13: Analysis of two kindreds;Bloom;Amer. J. hum. Genet.,1968

2. Mongolism by tertiary trisomy;Changantr;Lancet,1975

3. Trisomy for the proximal segment of the long arm chromosome 13. A new entity;Escobar;Amer. J. Dis. Child.,1974

4. Partial trisomy 13 plus partial trisomy 4q due to unusual segregation of translocation chromosomes;Fonatsch;Clin. Genet.,1979

5. Siblings with different types of chromosomal aberrations due to D/E trans-location of the mother;Hauschtek;Cytogenetics,1966

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1. Distal trisomy 3q as a risk factor for neural tube defects;Taiwanese Journal of Obstetrics and Gynecology;2016-10

2. Clinical delineation of proximal and distal partial 13q trisomy;Clinical Genetics;2008-04-23

3. C;Taybi and Lachman's Radiology of Syndromes, Metabolic Disorders and Skeletal Dysplasias;2007

4. Sonographic findings with pfeiffer syndrome;Prenatal Diagnosis;1994-01

5. Familial t(11;13)(q21;q14) and the duplication 11q, 13q phenotype;American Journal of Medical Genetics;1993-01-01
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