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American Journal of Medical Genetics|March 9, 1999
Congenital stapes ankylosis, broad thumbs, and hyperopia: report of a family and refinement of a syndromeJ Milunsky, C Suntra, C B MacDonald
Fetal Diagnosis and Therapy|August 26, 1998
Prenatal diagnosis for Schmid metaphyseal chondrodysplasia in twinsJ Milunsky, T Maher, R Lebo, et al.
Clinical Genetics|August 18, 1999
Schizophrenia susceptibility gene locus at Xp22.3J Milunsky, X L Huang, H E Wyandt, et al.
Clinical Genetics|August 31, 1999
A locus for autosomal recessive achromatopsia on human chromosome 8qA Milunsky, X L Huang, J Milunsky, et al.
Cancer Genetics and Cytogenetics|November 3, 1998
Evidence for genetic heterogeneity of the Carney complex (familial atrial myxoma syndromes)J Milunsky, X L Huang, C T Baldwin, et al.
Human Reproduction (Oxford, England)|February 7, 2001
Unilateral renal agenesis associated with congenital bilateral absence of the vas deferens: phenotypic findings and genetic considerationsT McCallum, J Milunsky, R Munarriz, et al.
American Journal of Medical Genetics|July 16, 1999
Symmetric replication of an unstable isodicentric Xq chromosome derived from isolocal maternal sister chromatid recombinationR V Lebo, J Milunsky, A W Higgins, et al.
American Journal of Medical Genetics|September 19, 1997
Familial paragangliomas: linkage to chromosome 11q23 and clinical implicationsJ Milunsky, A L DeStefano, X L Huang, et al.
American Journal of Medical Genetics|April 1, 1993
Characterization of a duplication in the terminal band of 4p by molecular cytogeneticsH E Wyandt, J Milunsky, T Lerner, et al.
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