Identification and evaluation of mental retardation von Daily, D K, Ardinger, H H, Holmes, G E

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Genotypic and phenotypic analysis of 396 individuals with mutations in Sonic Hedgehog von Solomon, Benjamin D, Bear, Kelly A, Wyllie, Adrian, Keaton, Amelia A, Dubourg, Christele, David, Veronique, Mercier, Sandra, Odent, Sylvie, Hehr, Ute, Paulussen, Aimee, Clegg, Nancy J, Delgado, Mauricio R, Bale, Sherri J, Lacbawan, Felicitas, Ardinger, Holly H, Aylsworth, Arthur S, Bhengu, Ntombenhle Louisa, Braddock, Stephen, Brookhyser, Karen, Burton, Barbara, Gaspar, Harald, Grix, Art, Horovitz, Dafne, Kanetzke, Erin, Kayserili, Hulya, Lev, Dorit, Nikkel, Sarah M, Norton, Mary, Roberts, Richard, Saal, Howard, Schaefer, G B, Schneider, Adele, Smith, Erika K, Sowry, Ellen, Spence, M Anne, Shalev, Stavit A, Steiner, Carlos E, Thompson, Elizabeth M, Winder, Thomas L, Balog, Joan Z, Hadley, Donald W, Zhou, Nan, Pineda-Alvarez, Daniel E, Roessler, Erich, Muenke, Maximilian

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Aggressive juvenile polyposis in children with chromosome 10q23 deletion von Septer, Seth, Zhang, Lei, Lawson, Caitlin E, Cocjin, Jose, Attard, Thomas, Ardinger, Holly H

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Comprehensive ZEB2 gene analysis for Mowat–Wilson syndrome in a North American cohort: A suggested approach to molecular diagnostics von Saunders, Carol J., Zhao, Weiwei, Ardinger, Holly H.

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Family history and clefting as major criteria for CHARGE syndrome von Hughes, Susan Starling, Welsh, Holly I., Safina, Nicole P., Bejaoui, Khemissa, Ardinger, Holly H.

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Association of genetic variation of the transforming growth factor-alpha gene with cleft lip and palate von ARDINGER, H. H, BUETOW, K. H, BELL, G. I, BARDACH, J, VANDEMARK, D. R, MURRAY, J. C

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Heterozygous deletion of the linked genes ZIC1 and ZIC4 is involved in Dandy-Walker malformation von Millen, Kathleen J, Grinberg, Inessa, Northrup, Hope, Ardinger, Holly, Prasad, Chitra, Dobyns, William B

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CDKN1C mutations and genital anomalies von Welsh, Holly I., Stockley, Tracy L., Parkinson, Nicole, Ardinger, Holly H.

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Expanding the phenotype of oculoectodermal syndrome: Possible relationship to encephalocraniocutaneous lipomatosis von Ardinger, Holly H., Horii, Kimberly A., Begleiter, Michael L.

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Classification of cardiovascular malformations associated with neuroblastoma von Lin, Angela, Ardinger, Holly H., Pierpont, Mary Ella

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Clinical presentation of velo-cardio-facial syndrome von Ardinger, Holly H, Ardinger, Robert H

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Association of transforming growth-factor alpha gene polymorphisms with nonsyndromic cleft palate only (CPO) von Shiang, R, Lidral, A C, Ardinger, H H, Buetow, K H, Romitti, P A, Munger, R G, Murray, J C

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Petty syndrome and Fontaine–Farriaux syndrome: Delineation of a single syndrome von Braddock, Stephen R., Ardinger, Holly H., Yang, Chun‐Song, Paschal, Bryce M., Hall, Bryan D.

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Historical perspectives of velo-cardio-facial syndrome von Ardinger, Holly H, Ardinger, Robert H

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RFLP for the human transforming growth factor beta-1 gene (TGFB) on chromosome 19 von ARDINGER, H. H, ARDINGER, R. H, BELL, G. I, MURRAY, J. C

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Linkage of an autosomal dominant clefting syndrome (Van der Woude) to Loci on chromosome Iq von MURRAY, J. C, NISHIMURA, D. Y, GLINSKI, L. P, PAULI, R. M, NAKAMURA, Y, GREEN, P. P, SCHINZEL, A, BUETOW, K. H, ARDINGER, H. H, SPENCE, M. A, SPARKES, R. S, FALK, R. E, FALK, P. M, GARDNER, R. J. M, HARKNESS, E. M

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Iodixanol pharmacokinetics in children von Johnson , Jr, W H, Lloyd, T R, Victorica, B E, Zales, V R, Epstein, M L, Leff, R D, Ardinger , Jr, R H, Slovis, T L, Johnson, J A, Marsters, P A

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Cardiovascular malformations in Smith-Lemli-Opitz syndrome von Lin, Angela E., Ardinger, Holly H., Ardinger Jr, Robert H., Cunniff, Christopher, Kelley, Richard I.

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The Hunter–MacDonald syndrome with expanded phenotype including risk of meningioma: An update and review von Armstrong, Linlea, Graham, Gail E., Schimke, R. Neil, Collins, Debra L., Kirse, Daniel J., Costello, Fiona, Ardinger, Holly H.

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Maternal serum screening and 22q11.2 deletion syndrome von Begleiter, Michael L., Lund, Molly M., Atherton, Andrea M., Buchholz, Janda D., Ardinger, Holly H.

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