Obesity and abnormal behaviour associated with interstitial deletion of chromosome 18 (q12.2q21.1).

Author:

Wilson G N,Al Saadi A A

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference4 articles.

1. Catalogue of unbalanced chromosome aberrations in man;Schinzel, A.,1984

2. Syndromes associated with deletion of the long arm of chromosome 18 [del(18q)];Wilson, M.G.; Towner, J.W.; Forsman, I.; Siris, E.;Am J Med Genet,1979

3. Familial mental retardation in a family with an inherited chromosome rearrangement;Chudley, A.E.; Bauder, F.; Ray, M.; McAlpine, P.J.; Pena, S.D.J.; Hamerton, J.L.;J Med Genet,1974

4. A six month old dysmorphic female was found to have partial trisomy for the long arm of chromosome 16 owing to a maternal translocation: 46, XX, t(9; 16)(p24; q21);Revised version accepted for publication,1988

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1. Syndromic obesity with neurodevelopmental delay: Opportunities for targeted interventions;European Journal of Medical Genetics;2022-03

2. Prenatal diagnosis and molecular cytogenetic characterization of an interstitial deletion of 18q12.1-q12.3 encompassing DTNA , CELF4 and SETBP1;Taiwanese Journal of Obstetrics and Gynecology;2017-12

3. Familial 18q12.2 deletion supports the role of RNA-binding protein CELF4 in autism spectrum disorders;American Journal of Medical Genetics Part A;2017-04-13

4. Features of Two Cases with 18q Deletion Syndrome;Journal of Clinical Research in Pediatric Endocrinology;2014-03-05

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