Your search returned 33 results.

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	1.	Breast-feeding during colchicine therapy for familial Mediterranean fever. [electronic resource] by Milunsky, J M Producer: 19910812 In: The Journal of pediatrics vol. 119 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Genetic counseling in perinatal medicine. [electronic resource] by Milunsky, J M Milunsky, A Producer: 19970529 In: Obstetrics and gynecology clinics of North America vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Case report: cystic fibrosis and embryonal carcinoma of the testis. [electronic resource] by Milunsky, J M Milunsky, A Producer: 19960506 In: The American journal of the medical sciences vol. 311 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Unmasking Kabuki syndrome: chromosome 8p22-8p23.1 duplication revealed by comparative genomic hybridization and BAC-FISH. [electronic resource] by Milunsky, J M Huang, X L Producer: 20040720 In: Clinical genetics vol. 64 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Prenatal diagnosis of spinal muscular atrophy by direct molecular analysis: efficacy and potential pitfalls. [electronic resource] by Milunsky, J M Cheney, S M Producer: 19991027 In: Genetic testing vol. 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Kabuki syndrome in a Haitian patient. [electronic resource] by Milunsky, J M Cheney, S M Producer: 20010524 In: American journal of medical genetics vol. 100 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Cerebro-oculo-facial-lymphatic syndrome. [electronic resource] by Milunsky, J M Capin, D M Producer: 20040203 In: Clinical genetics vol. 63 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Presymptomatic and prenatal diagnosis of myotonic muscular dystrophy with linked DNA probes. [electronic resource] by Milunsky, J M Skare, J C Milunsky, A Producer: 19910503 In: The American journal of the medical sciences vol. 301 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Familial supernumerary chromosome and malignancy. [electronic resource] by Milunsky, J M Wyandt, H E Milunsky, A Producer: 19960830 In: Cancer genetics and cytogenetics vol. 89 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Emerging phenotype of duplication (7p): a report of three cases and review of the literature. [electronic resource] by Milunsky, J M Wyandt, H E Milunsky, A Producer: 19891117 In: American journal of medical genetics vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Renal tubular dysgenesis with microcephaly. [electronic resource] by Milunsky, J M Genest, D R Milunsky, A Producer: 19970925 In: Pediatric nephrology (Berlin, Germany) vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Autism spectrum disorders: clinical and research frontiers. [electronic resource] by Caronna, E B Milunsky, J M Tager-Flusberg, H Producer: 20080620 In: Archives of disease in childhood vol. 93 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Rett syndrome from quintuple and triple deletions within the MECP2 deletion hotspot region. [electronic resource] by Lebo, R V Ikuta, T Milunsky, J M Milunsky, A Producer: 20011004 In: Clinical genetics vol. 59 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	The value of MLPA in Waardenburg syndrome. [electronic resource] by Milunsky, J M Maher, T A Ito, M Milunsky, A Producer: 20070906 In: Genetic testing vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Agenesis or hypoplasia of major salivary and lacrimal glands. [electronic resource] by Milunsky, J M Lee, V W Siegel, B S Milunsky, A Producer: 19910131 In: American journal of medical genetics vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Novel mutations and the emergence of a common mutation in the SDHD gene causing familial paraganglioma. [electronic resource] by Milunsky, J M Maher, T A Michels, V V Milunsky, A Producer: 20010823 In: American journal of medical genetics vol. 100 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	Connexin-26 gene analysis in hearing-impaired newborns. [electronic resource] by Milunsky, J M Maher, T A Yosunkaya, E Vohr, B R Producer: 20010329 In: Genetic testing vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	Delineation of a supernumerary marker chromosome utilizing a multimodal approach of G-banding, fluorescent in situ hybridization, confirmatory P1 artificial chromosome fluorescent in situ hybridization, and high-resolution comparative genomic hybridization. [electronic resource] by Mark, H F L Wyandt, H Huang, X L Milunsky, J M Producer: 20050913 In: Clinical genetics vol. 68 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	Highly polymorphic short tandem repeat analyses clarify complex molecular test results. [electronic resource] by Lebo, R V Maher, T Farrer, L Fenerci, E Y Milunsky, J M Producer: 20020206 In: Diagnostic molecular pathology : the American journal of surgical pathology, part B vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	LADD syndrome is caused by FGF10 mutations. [electronic resource] by Milunsky, J M Zhao, G Maher, T A Colby, R Everman, D B Producer: 20060628 In: Clinical genetics vol. 69 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 33 results.