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	141.	[Oculo-dento-digital dysplasia. (Observations in mother and child)]. [electronic resource] by Pfeiffer, R A Erpenstein, H Jünemann, G Producer: 19681024 In: Klinische Monatsblatter fur Augenheilkunde vol. 152 Availability: No items available. Save to lists Add to cart (remove)
	142.	[Chromosome anomalies caused by surplus (trisomies) and age of the mother]. [electronic resource] by Lenz, W Pfeiffer, R A Tünte, W Producer: 19661015 In: Deutsche medizinische Wochenschrift (1946) vol. 91 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	143.	Femoral duplication and the developmental field. [electronic resource] by Pfeiffer, R A Suess, J Schrott, K M Producer: 19900927 In: American journal of medical genetics vol. 36 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	144.	Clotting factors VII and X as useful markers of terminal deletion of chromosome 13. [electronic resource] by Pfeiffer, R A Ott, R Taben, K D Producer: 19850425 In: Human genetics vol. 69 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	145.	[Reciprocal translocation between a chromosome number 21 (G1) and a chromosome of the group C(C6)]. [electronic resource] by Pfeiffer, R A Laermann, J Heidtmann, H L Producer: 19680913 In: Helvetica paediatrica acta vol. 22 Availability: No items available. Save to lists Add to cart (remove)
	146.	Short stature, mental retardation and multiple dysmorphisms in two unrelated females: one or two different syndromes or none? [electronic resource] by Pfeiffer, R A Kapferer, L Tietze, H U Producer: 19970303 In: Genetic counseling (Geneva, Switzerland) vol. 7 Availability: No items available. Save to lists Add to cart (remove)
	147.	[Genetic-morphologic fatal syndromes]. [electronic resource] by Pfeiffer, R A Henkel, K E Stöss, H Producer: 19940407 In: Der Pathologe vol. 14 Availability: No items available. Save to lists Add to cart (remove)
	148.	[Fatal genetic-morphologic syndromes. Fatal pterygium syndrome]. [electronic resource] by Henkel, K E Pfeiffer, R A Stöss, H Producer: 19930719 In: Der Pathologe vol. 14 Availability: No items available. Save to lists Add to cart (remove)
	149.	Ring chromosome 18 (46, XX, 18r). [electronic resource] by Cenani, A Pfeiffer, R A Simon, H A Producer: 19700305 In: Humangenetik vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	150.	[Genetic-morphologic fatal syndromes. Cerebro-oculo-facioskeletal syndrome (Pena-Shokeir syndrome II)]. [electronic resource] by Henkel, K E Pfeiffer, R A Stöss, H Producer: 19931007 In: Der Pathologe vol. 14 Availability: No items available. Save to lists Add to cart (remove)
	151.	[Genetic-morphologic fatal syndromes. Bowen-Conradi syndrome]. [electronic resource] by Henkel, K E Pfeiffer, R A Stöss, H Producer: 19931007 In: Der Pathologe vol. 14 Availability: No items available. Save to lists Add to cart (remove)
	152.	[Fatal genetic-morphologic syndromes. The campomelic syndrome]. [electronic resource] by Henkel, K E Pfeiffer, R A Stöss, H Producer: 19930719 In: Der Pathologe vol. 14 Availability: No items available. Save to lists Add to cart (remove)
	153.	[Genetic morphological fatal syndromes. The Fryns syndrome]. [electronic resource] by Henkel, K E Pfeiffer, R A Stöss, H Producer: 19930513 In: Der Pathologe vol. 14 Availability: No items available. Save to lists Add to cart (remove)
	154.	[Genetic morphological fatal syndromes. The cryptophthalmos syndrome (Fraser syndrome)]. [electronic resource] by Henkel, K E Pfeiffer, R A Stöss, H Producer: 19930513 In: Der Pathologe vol. 14 Availability: No items available. Save to lists Add to cart (remove)
	155.	[The campomelic syndrome (author's transl)]. [electronic resource] by Berndt, K J Seiler, R Pfeiffer, R A Producer: 19760520 In: Monatsschrift fur Kinderheilkunde vol. 124 Availability: No items available. Save to lists Add to cart (remove)
	156.	Interstitial deletion of chromosome 9q with coexistence of the deleted segment as a ring chromosome. A case report. [electronic resource] by Pfeiffer, R A Trautmann, U Hirmer-Stoll, R Producer: 19920521 In: Annales de genetique vol. 34 Availability: No items available. Save to lists Add to cart (remove)
	157.	Mosaicism of a microdeletion of 486 bp involving the CGG repeat of the FMR1 gene due to misalignment of GTT tandem repeats at chi-like elements flanking both breakpoints and a full mutation. [electronic resource] by Schmucker, B Ballhausen, W G Pfeiffer, R A Producer: 19961015 In: Human genetics vol. 98 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	158.	[Autosome dominant vitreoretinal dystrophy with skeletal dysplasia in one generation]. [electronic resource] by Lang, G E Laudi, B Pfeiffer, R A Producer: 19910731 In: Klinische Monatsblatter fur Augenheilkunde vol. 198 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	159.	An autosomal dominant facio-audio symphalangism syndrome with Klippel-Feil anomaly: a new variant of multiple synostoses. [electronic resource] by Pfeiffer, R A Rott, H D Angerstein, W Producer: 19910503 In: Genetic counseling (Geneva, Switzerland) vol. 1 Availability: No items available. Save to lists Add to cart (remove)
	160.	Aplasia of the thumbs and great toes as the outstanding feature of Yunis and Varon syndrome. A new entity. A new observation. [electronic resource] by Pfeiffer, R A Diekmann, L Stock, H J Producer: 19890309 In: Annales de genetique vol. 31 Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 274 results.