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	61.	The van der Woude syndrome in a large kindred: variability, penetrance, genetic risks. [electronic resource] by Janku, P Robinow, M Kelly, T Bralley, R Baynes, A Edgerton, M T Producer: 19800923 In: American journal of medical genetics vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	62.	Autosomal dominant ectrodactyly and absence of long bones of upper or lower limbs: further clinical delineation. [electronic resource] by Hoyme, H E Jones, K L Nyhan, W L Pauli, R M Robinow, M Producer: 19871113 In: The Journal of pediatrics vol. 111 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	63.	The first seriatim study of human growth and middle aging. [electronic resource] by Roche, A F Garn, S M Reynolds, E L Robinow, M Sontag, L W Producer: 19810723 In: American journal of physical anthropology vol. 54 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	64.	Discordance in monozygotic twins for aglossia-adactylia, and possible clues to the pathogenesis of the syndrome. [electronic resource] by Robinow, M Marsh, J L Edgerton, M T Sabio, H Johnson, G F Producer: 19790313 In: Birth defects original article series vol. 14 Availability: No items available. Save to lists Add to cart (remove)
	65.	Metacarpophalangeal pattern profile analysis in Robinow syndrome. [electronic resource] by Butler, M G Gale, D D Meaney, F J Wadlington, W B Robinow, M Producer: 19870724 In: American journal of medical genetics vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	66.	Distal 15q trisomy: phenotypic comparison of nine cases in an extended family. [electronic resource] by Schnatterly, P Bono, K L Robinow, M Wyandt, H E Kardon, N Kelly, T E Producer: 19840502 In: American journal of human genetics vol. 36 Availability: No items available. Save to lists Add to cart (remove)
	67.	The Weissenbacher-Zweymuller syndrome of micrognathia and rhizomelic chondrodysplasia at birth with subsequent normal growth. [electronic resource] by Haller, J O Berdon, W E Robinow, M Slovis, T L Baker, D H Johnson, G F Producer: 19760401 In: The American journal of roentgenology, radium therapy, and nuclear medicine vol. 125 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	68.	Acrodysostosis. A syndrome of peripheral dysostosis, nasal hypoplasia, and mental retardation. [electronic resource] by Robinow, M Pfeiffer, R A Gorlin, R J McKusick, V A Renuart, A W Johnson, G F Summitt, R L Producer: 19710530 In: American journal of diseases of children (1960) vol. 121 Availability: No items available. Save to lists Add to cart (remove)
	69.	Systemic membrane defect in the proximal muscular dystrophies. [electronic resource] by Pickard, N A Gruemer, H D Verrill, H L Isaacs, E R Robinow, M Nance, W E Myers, E C Goldsmith, B Producer: 19781202 In: The New England journal of medicine vol. 299 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	70.	Secondary trisomy or mosaic "tetrasomy" 8p. [electronic resource] by Robinow, M Haney, N Chen, H Sorauf, T Van Dyke, D L Babu, V R Powell, S Maliszewski, W Guerin, S Landers, J W Producer: 19890630 In: American journal of medical genetics vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	71.	Diagnostic criteria for Walker-Warburg syndrome. [electronic resource] by Dobyns, W B Pagon, R A Armstrong, D Curry, C J Greenberg, F Grix, A Holmes, L B Laxova, R Michels, V V Robinow, M Producer: 19890427 In: American journal of medical genetics vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	72.	Ehlers-Danlos syndrome type VIIA and VIIB result from splice-junction mutations or genomic deletions that involve exon 6 in the COL1A1 and COL1A2 genes of type I collagen. [electronic resource] by Byers, P H Duvic, M Atkinson, M Robinow, M Smith, L T Krane, S M Greally, M T Ludman, M Matalon, R Pauker, S Quanbeck, D Schwarze, U Producer: 19971020 In: American journal of medical genetics vol. 72 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	73.	Mucolipidosis III (pseudo-Hurler polydystrophy): Clinical and laboratory studies in a series of 12 patients. [electronic resource] by Kelly, T E Thomas, G H Taylor, H A McKusick, V A Sly, W S Glaser, J H Robinow, M Luzzatti, L Espiritu, C Feingold, M Bull, M J Ashenhurst, E M Ives, E J Producer: 19760114 In: The Johns Hopkins medical journal vol. 137 Availability: No items available. Save to lists Add to cart (remove)