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Clinical Genetics|January 23, 2009
Noncoding RNAs in mental retardationK E Szulwach, P Jin, R S AlischClinical Genetics|January 23, 2009
Prevalence of dural ectasia in 63 gene-mutation-positive patients with features of Marfan syndrome type 1 and Loeys-Dietz syndrome and report of 22 novel FBN1 mutationsB Söylen, K K Singh, A Abuzainin, et al.Clinical Genetics|October 19, 2010
Identification of disease-associated DNA methylation in intestinal tissues from patients with inflammatory bowel diseaseZ Lin, J P Hegarty, J A Cappel, et al.Clinical Genetics|October 19, 2010
Two novel WTX mutations underscore the unpredictability of male survival in osteopathia striata with cranial sclerosisB Perdu, P Lakeman, G Mortier, et al.Clinical Genetics|November 3, 2010
CCMG guidelines: prenatal and postnatal diagnostic testing for uniparental disomyA J Dawson, J Chernos, J McGowan-Jordan, et al.Clinical Genetics|April 5, 2013
Gonadal mosaicism as a rare cause of autosomal recessive inheritanceS Anazi, E Al-Sabban, F S AlkurayaClinical Genetics|January 17, 2013
MLL2 mutation detection in 86 patients with Kabuki syndrome: a genotype-phenotype studyP Makrythanasis, B W van Bon, M Steehouwer, et al.Clinical Genetics|January 17, 2013
Fragile X syndrome: clinical, cytogenetic and molecular screening among autism spectrum disorder children in IndonesiaT I Winarni, A Utari, F E P Mundhofir, et al.Clinical Genetics|January 18, 2013
Variants of uncertain significance in BRCA testing: evaluation of surgical decisions, risk perception, and cancer distressJ O Culver, C D Brinkerhoff, J Clague, et al.Clinical Genetics|February 6, 2013
An emerging role for Wnt and GSK3 signaling pathways in schizophreniaK K SinghPageof 718