Oculo-Ectodermal Syndrome: Report of a Case With Mosaicism for a Deletion on Xq12FICKIE, Matthew R; STOLER, Joan M.American journal of medical genetics. Part A. 2011, Vol 155, Num 12, pp 3122-3124, issn 1552-4825, 3 p.Article

Recognition of facial features of fetal alcohol syndrome in the newbornSTOLER, Joan Marilyn; HOLMES, Lewis Ball.American journal of medical genetics. 2004, Vol 127c, Num 1, pp 21-27, issn 0148-7299, 7 p.Article

Patients with Ehlers Danlos syndrome and CRPS : A possible association?STOLER, Joan M; OAKLANDER, Anne Louise.Pain (Amsterdam). 2006, Vol 123, Num 1-2, pp 204-209, issn 0304-3959, 6 p.Article

Alcohol dehydrogenase 2 genotypes, maternal alcohol use, and infant outcomeSTOLER, Joan M; RYAN, Louise M; HOLMES, Lewis B et al.The Journal of pediatrics. 2002, Vol 141, Num 6, pp 780-785, issn 0022-3476, 6 p.Article

The Frequency of Palatal Anomalies in Saethre-Chotzen SyndromeSTOLER, Joan M; ROGERS, Gary F; MULLIKEN, John B et al.The Cleft palate-craniofacial journal. 2009, Vol 46, Num 3, pp 280-284, issn 1055-6656, 5 p.Article

Case 36-2004: A 23-day-old infant with hypospadias and failure to thriveSTOLER, Joan M; LEACH, Natalia T; DONAHOE, Patricia K et al.The New England journal of medicine. 2004, Vol 351, Num 22, pp 2319-2326, issn 0028-4793, 8 p.Article

A genome-wide association study identifies susceptibility loci for nonsyndromic sagittal craniosynostosis near BMP2 and within BBS9JUSTICE, Cristina M; YAGNIK, Garima; KIMONIS, Virginia et al.Nature genetics. 2012, Vol 44, Num 12, pp 1360-1364, issn 1061-4036, 5 p.Article

FOXE3 Plays a Significant Role in Autosomal Recessive MicrophthalmiaREIS, Linda M; TYLER, Rebecca C; SCHNEIDER, Adele et al.American journal of medical genetics. Part A. 2010, Vol 152, Num 3, pp 582-590, issn 1552-4825, 9 p.Article

Magnetic Resonance Imaging for Detection of Brain Abnormalities in Fetuses With Cleft Lip and/or Cleft PalateROSEN, Heather; CHIOU, Grace J; STOLER, Joan M et al.The Cleft palate-craniofacial journal. 2011, Vol 48, Num 5, pp 619-622, issn 1055-6656, 4 p.Article

Audiologic Findings in Saethre-Chotzen SyndromeROSEN, Heather; ANDREWS, Brian T; MEARA, John G et al.Plastic and reconstructive surgery (1963). 2011, Vol 127, Num 5, pp 2014-2020, issn 0032-1052, 7 p.Article

Congenital malformations among infants born to women receiving montelukast, inhaled corticosteroids, and other asthma medicationsNELSEN, Linda M; SHIELDS, Kristine E; CUNNINGHAM, Michael L et al.Journal of allergy and clinical immunology. 2012, Vol 129, Num 1, pp 251-254, issn 0091-6749, 4 p.Article

Deletions in GRID2 lead to a recessive syndrome of cerebellar ataxia and tonic upgaze in humansHILLS, L. Benjamin; MASRI, Amira; NASIR, Ramzi et al.Neurology. 2013, Vol 81, Num 16, pp 1378-1386, issn 0028-3878, 9 p.Article

Deletions of NRXN1 (Neurexin-1) Predispose to a Wide Spectrum of Developmental DisordersCHING, Michael S. L; YIPING SHEN; AUSTIN, Christina et al.American journal of medical genetics. Part B, Neuropsychiatric genetics. 2010, Vol 153, Num 4, pp 937-947, issn 1552-4841, 11 p.Article

Molecular and clinical analyses of greig cephalopolysyndactyly and pallister-hall syndromes : Robust phenotype prediction from the type and position of GL13 mutationsJOHNSTON, Jennifer J; OLIVOS-GLANDER, Isabelle; BOOTH, Carol et al.American journal of human genetics. 2005, Vol 76, Num 4, pp 609-622, issn 0002-9297, 14 p.Article