Non‐immune hydrops fetalis is associated with bi‐allelic pathogenic variants in the MYB Binding Protein 1a (MYBBP1A) gene von Tenorio‐Castano, Jair, Mansilla Aparicio, Elena, García Santiago, Fe Amalia, Klotz, Cherise M., Regojo, Rita María, Anguita, Estefanía, Ryan, Erin, Juusola, Jane, Herrero, Beatriz, Arias, Pedro, Parra, Alejandro, Pascual, Patricia, Gallego, Natalia, Cazalla, Mario, Rodriguez‐González, Roberto, Antolín, Eugenia, Nevado, Julián, Ruiz‐Perez, Víctor L., Lapunzina, Pablo

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A Novel Deletion in the Thyrotropin Beta-Subunit Gene Identified by Array Comparative Genomic Hybridization Analysis Causes Central Congenital Hypothyroidism in a Boy Originating f... von Hermanns, Pia, Couch, Robert, Leonard, Norma, Klotz, Cherise, Pohlenz, Joachim

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Revisiting the recurrence risk of nonsyndromic cleft lip with or without cleft palate von Klotz, Cherise M., Wang, Xiaojing, DeSensi, Rebecca S., Grubs, Robin E., Costello, Bernard J., Marazita, Mary L.

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Addressing Diversity in the Genetic Counseling Profession von Klotz, Cherise M.

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Whorl patterns on the lower lip are associated with nonsyndromic cleft lip with or without cleft palate von Neiswanger, Katherine, Chirigos, Kevin W., Klotz, Cherise M., Cooper, Margaret E., Bardi, Kathleen M., Brandon, Carla A., Weinberg, Seth M., Vieira, Alexandre R., Martin, Rick A., Czeizel, Andrew E., Castilla, Eduardo E., Poletta, Fernando A., Marazita, Mary L.

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Sudden infant death syndrome (SIDS) in African Americans: polymorphisms in the gene encoding the stress peptide pituitary adenylate cyclase-activating polypeptide (PACAP) von Cummings, Kevin J, Klotz, Cherise, Liu, Wei-Qiao, Weese-Mayer, Debra E, Marazita, Mary L, Cooper, Margaret E, Berry-Kravis, Elizabeth M, Tobias, Rose, Goldie, Cameron, Bech-Hansen, N Torben, Wilson, Richard JA

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MG-140 17Q21.31 microdeletion syndrome: A description of two cases von Doonanco, Kurston, Klotz, Cherise, Chernos, Judy, Yoshimoto, Maisa, Jain, Shailly

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