Effect of Integrating Substance Use Disorder Treatment into Primary Care on Inpatient and Emergency Department Utilization von Wakeman, Sarah E., Rigotti, Nancy A., Chang, Yuchiao, Herman, Grace E., Erwin, Ann, Regan, Susan, Metlay, Joshua P.

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The prevalence of PTEN mutations in a clinical pediatric cohort with autism spectrum disorders, developmental delay, and macrocephaly von Varga, Elizabeth A., Pastore, Matthew, Prior, Thomas, Herman, Gail E., McBride, Kim L.

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Disorders of cholesterol biosynthesis: prototypic metabolic malformation syndromes von Herman, Gail E

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Medical complications in long-term survivors with X-linked myotubular myopathy von Herman, Gail E., Finegold, Milton, Zhao, Wei, de Gouyon, Beatrice, Metzenberg, Aida

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Characterization of mutations in fifty North American patients with X-linked myotubular myopathy von Herman, Gail E., Kopacz, Kevin, Zhao, Wei, Mills, Patti L., Metzenberg, Aida, Das, Soma

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Characterization of mutations in 22 females with X-linked dominant chondrodysplasia punctata (Happle syndrome) von Herman, Gail E., Kelley, Richard I., Pureza, V., Smith, D., Kopacz, Kevin, Pitt, James, Sutphen, Rebecca, Sheffield, Leslie J., Metzenberg, Aida B.

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Changes in gene expression associated with loss of function of the NSDHL sterol dehydrogenase in mouse embryonic fibroblasts von Cunningham, David, Swartzlander, Daniel, Liyanarachchi, Sandya, Davuluri, Ramana V, Herman, Gail E

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The X-linked mouse mutation Bent tail is associated with a deletion of the Zic3 locus von CARREL, T, PURANDARE, S. M, HARRISON, W, ELDER, F, FOX, T, CASEY, B, HERMAN, G. E

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Left‐sided CHILD syndrome caused by a nonsense mutation in the NSDHL gene von Hummel, Marybeth, Cunningham, David, Mullett, Charles J., Kelley, Richard I., Herman, Gail E.

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Placental defects are associated with male lethality in bare patches and striated embryos deficient in the NAD(P)H Steroid Dehydrogenase-like (NSDHL) Enzyme von Caldas, Hugo, Cunningham, David, Wang, Xiaojian, Jiang, Fenglei, Humphries, Leon, Kelley, Richard I., Herman, Gail E.

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The role of Zic3 in vertebrate development von Herman, G.E., El-Hodiri, H.M.

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Identification of two novel mutations in the murine Nsdhl sterol dehydrogenase gene and development of a functional complementation assay in yeast von Lucas, Marsha E, Ma, Qi, Cunningham, David, Peters, Jo, Cattanach, Bruce, Bard, Martin, Elmore, Bradley K, Herman, Gail E

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Physical Mapping of the Mouse Genome von Herman, Gail E.

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Some logical and syntactical observations concerning the first-order dependent type system λP von GEUVERS, HERMAN, BARENDSEN, ERIK

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exma: an X-linked insertional mutation that disrupts forebrain and eye development von Cunningham, David, Xiao, Qiang, Chatterjee, Aurobindo, Sulik, Kathleen, Juriloff, Diana, Elder, Frederick, Harrison, Wilbur, Schuster, Gabriele, Overbeek, Paul A, Herman, Gail E

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Genomic Structure of a Novel LIM Domain Gene (ZNF185) in Xq28 and Comparisons with the Orthologous Murine Transcript von Heiss, Nina S, Gloeckner, Gernot, Bächner, Dietmar, Kioschis, Petra, Klauck, Sabine M, Hinzmann, Bernd, Rosenthal, André, Herman, Gail E, Poustka, Annemarie

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Mutations in a Delta super(8)- Delta super(7) sterol isomerase in the tattered mouse and X-linked dominant chondrodysplasia punctata von Derry, JMJ, Gormally, E, Means, G D, Zhao, W, Meindl, A, Kelley, R I, Boyd, Y, Herman, GE

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Severe neurocognitive and growth disorders due to variation in THOC2, an essential component of nuclear mRNA export machinery von Kumar, R, Gardner, A, Homan, CC, Douglas, E, Mefford, H, Wieczorek, D, Lüdecke, HJ, Stark, Z, Sadedin, S, Nowak, CB, Douglas, J, Parsons, G, Mark, P, Loidi, L, Herman, GE, Mihalic Mosher, T, Gillespie, MK, Brady, L, Tarnopolsky, M, Madrigal, I, Eiris, J, Domènech Salgado, L, Rabionet, R, Strom, TM, Ishihara, N, Inagaki, H, Kurahashi, H, Dudding-Byth, T, Palmer, EE, Field, M, Gecz, J, Palmer, Elizabeth

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TERATOGENIC EFFECTS OF FIRST-TRIMESTER CYCLOPHOSPHAMIDE THERAPY von Kirshon, Brian, Wasserstrum, Nathan, Willis, Rita, Herman, Gail E, McCabe, Edward R. B

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Genetic and Physical Mapping of a Gene Encoding a Methyl CpG Binding Protein, Mecp2, to the Mouse X Chromosome von Quaderi, N.A., Meehan, R.R., Tate, P.H., Cross, S.H., Bird, A.P., Chatterjee, A., Herman, G.E., Brown, S.D.M.

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