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	1561.	Sympus apus. [electronic resource] by Malkasian, G D Sayre, G P Titus, J L Producer: 19690523 In: Obstetrics and gynecology vol. 33 Availability: No items available. Save to lists Add to cart (remove)
	1562.	Popliteal pterygium syndrome in a Swedish family--clinical findings and genetic analysis with the van der Woude syndrome locus at 1q32-q41. [electronic resource] by Wong, F K Gustafsson, B Producer: 20001113 In: Acta odontologica Scandinavica vol. 58 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1563.	Further clinical delineation in trisomy 1q32 syndrome. [electronic resource] by Nuño-Arana, I González-García, J R García-Cruz, D Producer: 20020221 In: Annales de genetique vol. 44 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1564.	Phenotype and genotype in Nicolaides-Baraitser syndrome. [electronic resource] by Sousa, Sérgio B Hennekam, Raoul C Producer: 20150727 In: American journal of medical genetics. Part C, Seminars in medical genetics vol. 166C Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1565.	Genome damage in children with classical Ehlers-Danlos syndrome - An in vivo and in vitro study. [electronic resource] by Aghajanyan, Anna Fucic, Aleksandra Tskhovrebova, Leila Gigani, Olga Konjevoda, Pasko Producer: 20200206 In: European journal of medical genetics vol. 62 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1566.	Prenatal diagnosis and dysmorphic findings in mosaic trisomy 16. [electronic resource] by Garber, A Carlson, D Schreck, R Fischel-Ghodsian, N Hsu, W T Oeztas, S Pepkowitz, S Graham, J M Producer: 19940920 In: Prenatal diagnosis vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1567.	Overexpression of insulin-like growth factor-1 induces hyperplasia, dermal abnormalities, and spontaneous tumor formation in transgenic mice. [electronic resource] by Bol, D K Kiguchi, K Gimenez-Conti, I Rupp, T DiGiovanni, J Producer: 19970523 In: Oncogene vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1568.	New developments in wound care for infants and children. [electronic resource] by Valencia, I C Falabella, A F Schachner, L A Producer: 20010823 In: Pediatric annals vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1569.	Bi-allelic AEBP1 mutations in two patients with Ehlers-Danlos syndrome. [electronic resource] by Syx, Delfien De Wandele, Inge Symoens, Sofie De Rycke, Riet Hougrand, Olivier Voermans, Nicol De Paepe, Anne Malfait, Fransiska Producer: 20200206 In: Human molecular genetics vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1570.	XXXXY syndrome in a phenotypic male infant with associated cardiac abnormalities. [electronic resource] by Assemany, S R Neu, R L Gardner, L I Producer: 19711106 In: Humangenetik vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1571.	Microphthalmia with linear skin defects (MLS) syndrome: clinical, cytogenetic, and molecular characterization. [electronic resource] by Lindsay, E A Grillo, A Ferrero, G B Roth, E J Magenis, E Grompe, M Hultén, M Gould, C Baldini, A Zoghbi, H Y Producer: 19940325 In: American journal of medical genetics vol. 49 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1572.	A four generation hidrotic ectodermal dysplasia family: an allelic variant of Clouston syndrome? [electronic resource] by Turnpenny, P D De Silva, D C Gregory, D W Gray, E S Dean, J C Producer: 19960312 In: Clinical dysmorphology vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1573.	Permeability barrier dysfunction in transgenic mice overexpressing claudin 6. [electronic resource] by Turksen, Kursad Troy, Tammy-Claire Producer: 20020524 In: Development (Cambridge, England) vol. 129 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1574.	Refinement and delineation of the breakpoint regions of a chromosome 1;22 translocation in a patient with Costello syndrome. [electronic resource] by Maróti, Zoltán Kutsche, Kerstin Sutajova, Marketa Gal, Andreas Nothwang, Hans Gerd Czeizel, Andrew E Tímár, László Sólyom, Enikö Producer: 20020808 In: American journal of medical genetics vol. 109 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1575.	[Trisomy 18 syndrome(Edwards syndrome)]. [electronic resource] by Ieshima, A Producer: 20010125 In: Ryoikibetsu shokogun shirizu no. 30 Pt 5 Availability: No items available. Save to lists Add to cart (remove)
	1576.	Biochemical characterization of novel germline BRAF and MEK mutations in cardio-facio-cutaneous syndrome. [electronic resource] by Rodriguez-Viciana, Pablo Rauen, Katherine A Producer: 20080619 In: Methods in enzymology vol. 438 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1577.	Arteriolar hyalinosis and arterial hypertension as possible surrogate markers of reduced interstitial blood flow and hypoxia in glomerulonephritis. [electronic resource] by Bazzi, Claudio Stivali, Gilda Rachele, Gregorio Rizza, Virginia Casellato, Daniela Nangaku, Masaomi Producer: 20150723 In: Nephrology (Carlton, Vic.) vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1578.	Intraspinal lesions associated with sacrococcygeal dimples. [electronic resource] by Harada, Atsuko Nishiyama, Kenichi Yoshimura, Junichi Sano, Masakazu Fujii, Yukihiko Producer: 20140901 In: Journal of neurosurgery. Pediatrics vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1579.	Mutation spectrum of NF1 gene in Italian patients with neurofibromatosis type 1 using Ion Torrent PGM™ platform. [electronic resource] by Calì, Francesco Chiavetta, Valeria Ruggeri, Giuseppa Piccione, Maria Selicorni, Angelo Palazzo, Daniela Bonsignore, Maria Cereda, Anna Elia, Maurizio Failla, Pinella Figura, Maria Grazia Fiumara, Agata Maitz, Silvia Luana Mandarà, Giuseppa Maria Mattina, Teresa Ragalmuto, Alda Romano, Corrado Ruggieri, Martino Salluzzo, Roberto Saporoso, Antonino Schepis, Carmelo Sorge, Giovanni Spanò, Maria Tortorella, Gaetano Romano, Valentino Producer: 20170210 In: European journal of medical genetics vol. 60 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1580.	Cellular and animal models of skin alterations in the autism-related ADNP syndrome. [electronic resource] by Mollinedo, Pilar Kapitansky, Oxana Gonzalez-Lamuño, Domingo Zaslavsky, Adi Real, Pedro Gozes, Illana Gandarillas, Alberto Fernandez-Luna, Jose L Producer: 20200724 In: Scientific reports vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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