Whole-exome/genome sequencing and genomics von Grody, Wayne W, Thompson, Barry H, Hudgins, Louanne

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ACMG position statement on prenatal/preconception expanded carrier screening von Grody, Wayne W., Thompson, Barry H., Gregg, Anthony R., Bean, Lora H., Monaghan, Kristin G., Schneider, Adele, Lebo, Roger V.

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Phenylalanine hydroxylase deficiency: diagnosis and management guideline von Vockley, Jerry, Andersson, Hans C, Antshel, Kevin M, Braverman, Nancy E, Burton, Barbara K, Frazier, Dianne M, Mitchell, John, Smith, Wendy E, Thompson, Barry H, Berry, Susan A

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Improving newborn screening follow-up in pediatric practices: quality improvement innovation network von Hinton, Cynthia F, Neuspiel, Daniel R, Gubernick, Ruth S, Geleske, Timothy, Healy, Jill, Kemper, Alex R, Lloyd-Puryear, Michele A, Saul, Robert A, Thompson, Barry H, Kaye, Celia I

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Therapies for Inborn Errors of Metabolism: What Has the Orphan Drug Act Delivered? von TALELE, Sonali S, KUI XU, PARISER, Anne R, BRAUN, M. Miles, FARAG-EI-MASSAH, Sheiren, PHILLIPS, M. Ian, THOMPSON, Barry H, COTE, Timothy R

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ACMG Position Statement on Prenatal/Preconception Expanded Carrier Screening von Grody, Wayne W, Thompson, Barry H, Gregg, Anthony R, Bean, Lora H, Monaghan, Kristin G, Schneider, Adele, Lebo, Roger V

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Whole-exome/genome sequencing and genomics von Hudgins, Louanne, Thompson, Barry H, Grody, Wayne W

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Nelson Essentials of Pediatrics-Third Edition von Thompson, Barry H.

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Where Have All My Pumpkins Gone?: The Vulnerability of Insect Pollinatorsa von THOMPSON, BARRY H.

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Where Have All My Pumpkins Gone?: The Vulnerability of Insect Pollinators von THOMPSON, BARRY H.

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Duty to re-contact von Hirschhorn, K, Fleisher, L D, Godmilow, L, Howell, R R, Lebel, R R, McCabe, E R, McGinniss, M J, Milunsky, A, Pelias, M Z, Pyeritz, R E, Sujansky, E, Thompson, B H, Zinberg, R E

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Guidelines for expert witness testimony for the specialty of medical genetics. Social, Ethical and Legal Issues Committee, American College of Medical Genetics von McGinniss, Matthew J., Pelias, Mary Kay, Anderson, Rebecca R., Gelehrter, Thomas D., Godmilow, Lynn, Howell, R. Rodney, Thompson, Barry H.

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Detection of hemochromatosis through the analysis of single- nucleotide extension products by capillary electrophoresis von Liang, Q, Davis, P A, Simpson, J T, Thompson, B H, Devaney, J M, Girard, J

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Gastroschisis and omphalocele: Prenatal diagnosis and perinatal management von Davidson, J. M., Johnson Jr, Timothy R. B., Rigdon, David T., Thompson, Barry H.

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Hereditary deficiency of the third component of complement in a child with fever, skin rash, and arthralgias: Response to transfusion of whole blood von Osofsky, Stephen G., Thompson, Barry H., Lint, Thomas F., Gewurz, Henry

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FERTILITY AND 13/14 TRANSLOCATION von Palmer, CatherineG, Morris, JudithL, Thompson, BarryH, Nance, WalterE

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Evidence for lack of linkage between HLA and C3 deficiency in man von Osofsky, Stephen G., Thompson, Barry H., Gewurz, Henry, Schmid, Frank R., Mittal, Kamal K.

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Dominant preaxial brachydactyly with hallux varus and thumb abduction von Christian, J C, Cho, K S, Franken, E A, Thompson, B H

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Erythrocyte Diphosphopyridine Nucleotidase (NADase) in Paroxysmal Nocturnal Hemoglobinuria 1 von Thompson, Barry H., Hanna, Keith L., Van Eys, Jan, Hartmann, Robert C.

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Erythrocyte diphosphopyridine nucleotidase (NADase) in paroxysmal nocturnal hemoglobinuria von Thompson, B H, Hanna, K L, Van Eys, J, Hartmann, R C, Darby, W J

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