Carbohydrate metabolism in Turner's syndrome von Gruber, Dinah C., Harm, John P.

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Chromosome studies in full-term, low-birth-weight, mentally retarded patients von Chen, Andrew T.L., Sergovich, Frederick R., McKim, John S., Barr, Murray L., Gruber, Dinah

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XX/XY LYMPHOID CHIMÆRISM IN CONGENITAL IMMUNOLOGICAL DEFICIENCY SYNDROME WITH THYMIC ALYMPHOPLASIA von Kadowaki, Jun-Ichi, Thompson, RubyI, Zuelzer, WolfW, Woolley, PaulV, Joseph Brough, A., Gruber, Dinah

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The Newborn: CHROMOSOME STUDIES IN FULL TERM, LOW BIRTH WEIGHT, MENTALLY RETARDED PATIENTS von CHEN, ANDREW T. L, SERGOVICH, FREDERICK R, MCKIM, JOHN S, BARR, MURRAY L, GRUBER, DINAH

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PECONPI: A novel software for uncovering pathogenic copy number variations in non-syndromic sensorineural hearing loss and other genetically heterogeneous disorders von Tsai, Ellen A., Berman, Micah A., Conlin, Laura K., Rehm, Heidi L., Francey, Lauren J., Deardorff, Matthew A., Holst, Jenelle, Kaur, Maninder, Gallant, Emily, Clark, Dinah M., Glessner, Joseph T., Jensen, Shane T., Grant, Struan F.A., Gruber, Peter J., Hakonarson, Hakon, Spinner, Nancy B., Krantz, Ian D.

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