Prevalence of Childhood Permanent Hearing Loss after Early Complex Cardiac Surgery
Bork, Karin T., To, Beatrice P., Leonard, Norma J., Douglas, Charlotte M., Dinon, Diana A., Leonard, Elizabeth E., Valeriote, Hope A., Usher, Laurie F., Robertson, Charlene M.T.
Published in The Journal of pediatrics (01.07.2018)
Published in The Journal of pediatrics (01.07.2018)
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Two-year neurodevelopmental outcomes of infants undergoing neonatal cardiac surgery for interrupted aortic arch: A descriptive analysis
Joynt, Chloe A., MD, Robertson, Charlene M.T., MD, Cheung, Po-Yin, MD, PhD, Nettel-Aguirre, Alberto, PhD, Joffe, Ari R., MD, Sauve, Reg S., MD, Biggs, Wayne S.G., BA, Leonard, Norma J., MD, Ross, David B., MD, Rebeyka, Ivan M., MD
Published in The Journal of thoracic and cardiovascular surgery (01.10.2009)
Published in The Journal of thoracic and cardiovascular surgery (01.10.2009)
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Transmission of the rare HRAS mutation (c. 173C > T; p.T58I) further illustrates its attenuated phenotype
Gripp, Karen W., Hopkins, Elizabeth, Serrano, Alvaro, Leonard, Norma J., Stabley, Deborah L., Sol-Church, Katia
Published in American journal of medical genetics. Part A (01.05.2012)
Published in American journal of medical genetics. Part A (01.05.2012)
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Costello syndrome associated with novel germline HRAS mutations: An attenuated phenotype?
Gripp, Karen W., Innes, A. Micheil, Axelrad, Marni E., Gillan, Tanya L., Parboosingh, Jillian S., Davies, Christine, Leonard, Norma J., Lapointe, Monique, Doyle, Daniel, Catalano, Sarah, Nicholson, Linda, Stabley, Deborah L., Sol-Church, Katia
Published in American journal of medical genetics. Part A (15.03.2008)
Published in American journal of medical genetics. Part A (15.03.2008)
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Atypical facet of Möbius syndrome: Association with facioscapulohumeral muscular dystrophy
Kolski, Hanna K., Leonard, Norma J., Lemmers, Richard J.L.F., Bamforth, John S.
Published in Muscle & nerve (01.04.2008)
Published in Muscle & nerve (01.04.2008)
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Intracranial calcification, retinopathy, and osteopenia: a new syndrome?
Sazgar, Mona, Leonard, Norma J, Renaud, Deborah L, Bhargava, Ravi, Sinclair, D.Barry
Published in Pediatric neurology (01.04.2002)
Published in Pediatric neurology (01.04.2002)
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Prenatal diagnosis of del(15)(q26.1) and del(18)(q21.3) due to an unbalanced de novo translocation: ultrasound, molecular cytogenetic and autopsy findings
Froster, Ursula G., Horn, Lars-Christian, Holland, Heidrun, Strenge, Sibylle, Faber, Renaldo
Published in Prenatal diagnosis (01.12.2000)
Published in Prenatal diagnosis (01.12.2000)
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Polytopic anomalies with agenesis of the lower vertebral column
Bohring, A, Lewin, S O, Reynolds, J F, Voigtländer, T, Rittinger, O, Carey, J C, Köpernik, M, Smith, R, Zackai, E H, Leonard, N J, Gritter, H L, Bamforth, J S, Okun, N, McLeod, D R, Super, M, Powell, P, Mundlos, S, Hennekam, R C, van Langen, I M, Viskochil, D H, Wiedemann, H R, Opitz, J M
Published in American journal of medical genetics (19.11.1999)
Published in American journal of medical genetics (19.11.1999)
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