Roberts syndrome: clinical and cytogenetic aspects

Author:

Mann N P,Fitzsimmons J,Fitzsimmons E,Cooke P

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference7 articles.

1. A child with double cleft of lip and palate, protrusion of the intermaxillary portion of the upper jaw and an imperfect development of the bones of the four extremities;Roberts, J.B.,1919

2. The Roberts syndrome;Freeman, M.V.R.; Williams, D.W.; Schimke, N.; Temtamy, S.A.; Vachier, E.; German, J.;Clin Genet,1974

3. The SC phocomelia and Roberts syndrome: nosologic aspects;Herrmann, J.; Opitz, J.M.;Eur J Pediatr,1977

4. A sibship with pseudothalidomide syndrome and an association with Rh incompatability;Judge, C.;Med J Aust,1973

5. Cytological evidence for a disturbance in chromatid pairing;Stoll, C.; Levy, J.M.; Beshara, D.;Clin Genet; Roberts's syndrome and clonidine,1979

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1. Cohesin — bridging the gap among gene transcription, genome stability, and human diseases;FEBS Letters;2024-06-09

2. Roberts Syndrome;Atlas of Genetic Diagnosis and Counseling;2017

3. Roberts Syndrome;Atlas of Genetic Diagnosis and Counseling;2016

4. Roberts/SC Phocomelia Syndrome with Severe Tetra-Amelia: A Case Report;The Journal of Pediatric Research;2014-09-05

5. Roberts Syndrome;Atlas of Genetic Diagnosis and Counseling;2012

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