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	201.	[TWINS WITH MALFORMATIONS OF THE EXTREMITIES. THALIDOMIDE EMBRYOPATHY. III]. [electronic resource] by PFEIFFER, R A WEICKER, H BACHMANN, K D GLEISS, J Producer: 19961201 In: Deutsche medizinische Wochenschrift (1946) vol. 88 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	202.	[TWINS WITH MALFORMATIONS OF THE EXTREMITIES. THALIDOMIDE EMBRYOPATHY. 3]. [electronic resource] by PFEIFFER, R A WEICKER, H BACHMANN, K D GLEISS, J Producer: 19961201 In: Deutsche medizinische Wochenschrift (1946) vol. 88 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	203.	[Symptomatology of the ring chromosomes of the D group. (2 new observations of type 13r)]. [electronic resource] by Tolksdorf, M Goll, U Wiedemann, H R Pfeiffer, R A Producer: 19710209 In: Archiv fur Kinderheilkunde vol. 181 Availability: No items available. Save to lists Add to cart (remove)
	204.	[The XXXXY syndrome. Report of 7 new cases and review of the literature (author's transl)]. [electronic resource] by Terheggen, H G Pfeiffer, R A Haug, H Schünke, W Producer: 19740306 In: Zeitschrift fur Kinderheilkunde vol. 115 Availability: No items available. Save to lists Add to cart (remove)
	205.	[Thalidomide embryopathy. II. Results of individual anamnestic findings in the areas of inquiry of the universities of Bonn, Cologne, Muenster and Duesseldorf pediatric clinics]. [electronic resource] by WEICKER, H BACHMANN, K D PFEIFFER, R A GLEISS, J Producer: 19981101 In: Deutsche medizinische Wochenschrift (1946) vol. 87 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	206.	[Chromosome aberration 48, XXXY]. [electronic resource] by Pfeiffer, R A Wilking, H H Manz, F Krienitz, B Producer: 19730810 In: Munchener medizinische Wochenschrift (1950) vol. 115 Availability: No items available. Save to lists Add to cart (remove)
	207.	[Observations on the problem of sex-linked recessive mental retardation]. [electronic resource] by Neuhäuser, G Zerbin-Rüdin, E Pfeiffer, R A Klar, H Producer: 19691202 In: Archiv fur Psychiatrie und Nervenkrankheiten vol. 212 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	208.	Second-trimester diagnosis of fetal cataract in a fetus with Walker-Warburg syndrome. [electronic resource] by Beinder, E J Pfeiffer, R A Bornemann, A Wenkel, H Producer: 19971204 In: Fetal diagnosis and therapy vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	209.	A comparative ZOO-FISH analysis in bats elucidates the phylogenetic relationships between Megachiroptera and five microchiropteran families. [electronic resource] by Volleth, M Heller, K G Pfeiffer, R A Hameister, H Producer: 20030528 In: Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	210.	Subacute necrotizing encephalomyelopathy. Clinical, ultrastructural, biochemical and therapeutic studies in an infant. [electronic resource] by Gröbe, H Bassewitz, D B Dominick, H C Pfeiffer, R A Producer: 19751211 In: Acta paediatrica Scandinavica vol. 64 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	211.	[The oro-facial-digital syndrome. Symptoms and prognosis]. [electronic resource] by Majewski, F Lenz, W Pfeiffer, R A Tünte, W Müller, H Producer: 19720622 In: Zeitschrift fur Kinderheilkunde vol. 112 Availability: No items available. Save to lists Add to cart (remove)
	212.	Interstitial deletion del(3)(p12p21) in a malformed child subsequent to paternal paracentric insertion (or intraarm shift) 46,XY, ins(3)(p24.1p12.1p21.31). [electronic resource] by Pfeiffer, R A Rauch, A Ulmer, R Beinder, E Trautmann, U Producer: 19980625 In: Annales de genetique vol. 41 Availability: No items available. Save to lists Add to cart (remove)
	213.	Simultaneous de novo interstitial deletion of 16q21 and intercalary duplication of 19q in a retarded infant with minor dysmorphic features. [electronic resource] by Trautmann, U Pfeiffer, R A Seufert-Satomi, U Tietze, H U Producer: 19930610 In: Journal of medical genetics vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	214.	Absence of fibula and ulna with oligodactyly, contractures, right-angle bowing of femora, abnormal facial morphology, cleft lip/palate and brain malformation in two sibs: a possibly new lethal syndrome. [electronic resource] by Pfeiffer, R A Stöss, H Voight, H J Wündisch, G F Producer: 19880831 In: American journal of medical genetics vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	215.	Subdivision of the human Y chromosome. [electronic resource] by Jalal, S M Pfeiffer, R A Pathak, S Hsu, T C Producer: 19750131 In: Humangenetik vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	216.	RNA-based mutation screening in German families with Sjögren-Larsson syndrome. [electronic resource] by Kraus, C Braun-Quentin, C Ballhausen, W G Pfeiffer, R A Producer: 20000901 In: European journal of human genetics : EJHG vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	217.	Cytological analyses of 14p+ variant by means of N-banding and combinations of silver staining and chromosome bandings. [electronic resource] by Lau, Y F Wertelecki, W Pfeiffer, R A Arrighi, F E Producer: 19790611 In: Human genetics vol. 46 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	218.	[The clinical manifestations and cytogenetic observations of 7 cases affected by the cri-du-chat syndrome]. [electronic resource] by Mennicken, U Pfeiffer, R A Puyn, U Worbes, H Wagener, A Producer: 19690128 In: Zeitschrift fur Kinderheilkunde vol. 104 Availability: No items available. Save to lists Add to cart (remove)
	219.	Brachydactyly in a child with duplication-deficiency subsequent to t(15;20)(q25.2;p12.2)mat. Candidate regions on one or both chromosomes? [electronic resource] by Pfeiffer, R A Kändler, C Sieber, E Rauch, A Trautmann, U Producer: 19970819 In: Clinical genetics vol. 51 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	220.	Hypomelanosis of Ito (incontinentia pigmenti achromians). Ophthalmological evidence for somatic mosaicism. [electronic resource] by Rott, H D Lang, G E Huk, W Pfeiffer, R A Producer: 19910717 In: Ophthalmic paediatrics and genetics vol. 11 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 274 results.