|1.||Gerton, Jennifer L: 5 articles (03/2015 - 12/2008)|
|2.||Xu, Baoshan: 3 articles (03/2015 - 01/2013)|
|3.||Lu, Shuai: 2 articles (05/2014 - 01/2014)|
|4.||Lee, Kenneth K: 2 articles (05/2014 - 01/2013)|
|5.||Skibbens, Robert V: 2 articles (01/2013 - 04/2010)|
|6.||Mönnich, Maren: 2 articles (01/2012 - 01/2011)|
|7.||Horsfield, Julia A: 2 articles (01/2012 - 01/2011)|
|8.||Print, Cristin G: 2 articles (01/2012 - 01/2011)|
|9.||van der Lelij, Petra: 2 articles (02/2010 - 01/2010)|
|10.||de Winter, Johan P: 2 articles (02/2010 - 01/2010)|
01/01/2010 - "The importance of chromosome studies in Roberts syndrome/SC phocomelia and other cohesinopathies."
06/01/2012 - "Roberts syndrome and SC phocomelia (RBS/SC) are genetic autosomal recessive syndromes caused by establishment of cohesion 1 homolog 2 ( ESCO 2) mutation. "
06/01/2012 - "Establishment and characterization of Roberts syndrome and SC phocomelia model medaka (Oryzias latipes)."
04/15/2010 - "In humans, mutations in cohesion factors result in developmental abnormalities such as Cornelia de Lange, Roberts Syndrome/SC-Phocomelia, Rothman-Thompson Syndrome and others. "
02/01/2010 - "The Roberts syndrome/SC phocomelia spectrum--a case report of an adult with review of the literature."
|2.||Cleft Lip (Harelip)
09/23/1998 - "Bilaterally cleft lip, limb defects, and haematological manifestations: Roberts syndrome versus TAR syndrome."
10/31/1997 - "Tetraphocomelia and bilateral cleft lip in a historical case of Roberts syndrome [Virchow, 1898]."
05/01/1978 - "A clinicopathological study in a case of Roberts syndrome (tetraphocomelia, cleft lip and palate, and phallic hypertrophy) is reported. "
07/31/2000 - "Roberts syndrome (RS) is a rare autosomal recessive disorder characterized by heterogeneous clinical features, the most notable being tetraphocomelia, cleft lip, and cleft palate. "
02/15/2003 - "The findings of tetraphocomelia more severe in the upper limbs with reduction in the number and length of digits, hydrocephalus, bilateral cleft lip, micrognathia, and cryptorchidism are consistent with a diagnosis of Roberts syndrome. "
|4.||De Lange Syndrome (Cornelia De Lange Syndrome)
02/12/2010 - "The DDX11-deficient patient represents another cohesinopathy, besides Cornelia de Lange syndrome and Roberts syndrome, and shows that DDX11 functions at the interface between DNA repair and sister chromatid cohesion."
03/15/2015 - "Cohesinopathies are human genetic disorders that include Cornelia de Lange syndrome (CdLS) and Roberts syndrome (RBS) and are characterized by defects in limb and craniofacial development as well as mental retardation. "
01/01/2013 - "Roberts Syndrome (RBS) and Cornelia de Lange Syndrome (CdLS) are severe developmental maladies that present with nearly an identical suite of multi-spectrum birth defects. "
01/01/2012 - "Mutations in cohesin, or its regulators, cause a spectrum of human developmental syndromes known as the "cohesinopathies." Cohesinopathy disorders include Cornelia de Lange Syndrome and Roberts Syndrome. "
01/01/2011 - "The human developmental diseases Cornelia de Lange Syndrome (CdLS) and Roberts Syndrome (RBS) are both caused by mutations in proteins responsible for sister chromatid cohesion. "
|5.||Congenital Abnormalities (Deformity)
07/01/2011 - "Roberts syndrome is a genetically determined rare birth defect causing, skeletal deformities, particularly symmetrical limb reduction and craniofacial anomalies. "
01/01/2008 - "Roberts syndrome (Pseudothalidomide) is a rare birth defect that causes severe bone malformation complex. "
09/01/1996 - "Roberts syndrome (RS) is a rare, recessively inherited disorder characterized by growth retardation, limb reductions and craniofacial deformities. "
09/01/1991 - "Roberts syndrome (RS) is a rare recessive condition of limb deformities, growth retardation, and developmental delay. "
10/01/1989 - "Roberts syndrome (RS) is a rare genetic disorder, characterized clinically by severe pre- and post-natal growth retardation and symmetric limb reduction deformities. "
|3.||Craniosynostosis radial aplasia syndrome
|5.||Proteins (Proteins, Gene)
|6.||Milk Proteins (Milk Protein)
|8.||Ribosomal DNA (rDNA)
|9.||DNA (Deoxyribonucleic Acid)