Paternal transmission of fragile X syndrome von Zeesman, Susan, Zwaigenbaum, Lonnie, Whelan, Donald T., Hagerman, Randi J., Tassone, Flora, Taylor, Sherryl A.M.

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Pregnancy in a healthy woman with untreated citrullinemia von Potter, Murray A., Zeesman, Susan, Brennan, Barbara, Kobayashi, Keiko, Gao, Hong‐Zhi, Tabata, Ayako, Saheki, Takeyori, Whelan, Donald T.

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Smith-Lemli-Opitz syndrome: a treatable inherited error of metabolism causing mental retardation von Nowaczyk, Malgorzata J. M, Whelan, Donald T, Heshka, Timothy W, Hill, Robert E

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Oral‐facial‐digital syndrome VII is oral‐facial‐digital syndrome I: A clarification von Nowaczyk, Malgorzata J.M., Zeesman, Susan, Whelan, Donald T., Wright, Victoria, Feather, Sally A.

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Boy with 47,XXY,del(15)(q11.2q13) karyotype and Prader–Willi syndrome: A new case and review of the literature von Nowaczyk, Małgorzata J.M., Zeesman, Susan, Kam, April, Taylor, Sherryl A.M., Carter, Ronald F., Whelan, Donald T.

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Paternal transmission of the congenital form of myotonic dystrophy type 1: A new case and review of the literature von Zeesman, Susan, Carson, Nancy, Whelan, Donald T.

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Incidence of Smith-Lemli-Opitz syndrome in Ontario, Canada von Nowaczyk, Małgorzata J.M., McCaughey, Donna, Whelan, Donald T., Porter, Forbes D.

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Coping with dietary therapy in phenylketonuria: A case report von ARCHER, LYNDA A, CUNNINGHAM, CHARLES E, WHELAN, DONALD T

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No evidence of paternal transmission of fragile X syndrome von Steinbach, Doris, Steinbach, Peter

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Parents of children with spinal muscular atrophy are not obligate carriers: Carrier testing is important for reproductive decision-making von Zeesman, Susan, Whelan, Donald T., Carson, Nancy, McGowan-Jordan, Jean, Stockley, Tracy L., Ray, Peter N., Prior, Thomas W.

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Response to letter: "No evidence of paternal transmission of fragile X syndrome" by Doris and Peter Steinbach von Tassone, Flora, Zeesman, Susan, Zwaigenbaum, Lonnie, Whelan, Donald T., Hagerman, Randi J., Taylor, Sherryl A.M.

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Achondroplasia-hypochondroplasia complex in a newborn infant von Huggins, Marlene J., Smith, John R., Chun, Kathy, Ray, Peter N., Shah, Jay K., Whelan, Donald T.

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Hyperdibasicaminoaciduria: an inherited disorder of amino acid transport von Whelan, D T, Scriver, C R

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Glutamic Acid Decarboxylase and Gamma-aminobutyric Acid in Mammalian Kidney von WHELAN, DONALD T, SCRIVER, CHARLES R, MOHYUDDIN, FAZL

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Reply to correspondence from Martínez-Frías et al.-"Incidence of Smith-Lemli-Opitz syndrome in Ontario, Canada" von Nowaczyk, Małgorzata J.M., McCaughey, Donna, Whelan, Donald T., Porter, Forbes D.

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Maternal uniparental isodisomy of human chromosome 14 associated with a paternal t(13q14q) and precocious puberty von Tomkins, D J, Roux, A F, Waye, J, Freeman, V C, Cox, D W, Whelan, D T

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Smith-Lemli-Opitz syndrome: phenotypic extreme with minimal clinical findings von Nowaczyk, Malgorzata J.M., Whelan, Donald T., Hill, Robert E.

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Novel (cys152>arg) missense mutation in an Arab patient with Canavan disease von Kaul, Rajinder, Gao, Guang P., Michals, Kimberlee, Whelan, Donald T., Levin, Simon, Matalon, Reuben

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Incidence of Smith-Lemli-Opitz syndrome in Ontario, Canada von Martínez-Frías, M.L., Bermejo, E., Rodríguez-Pinilla, E.

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Postmortem protocol von WHELAN, DONALD T.

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