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	221.	[Are monozygous twins and twin-specific abnormalities more prevalent following extracorporeal fertilization? A comment on studies of the Gynecologic Clinic of the Erlangen-Nürnberg University]. [electronic resource] by Pfeiffer, R A Van Uem, J F Siebzehnrübl, E Wildt, L Producer: 19891221 In: Geburtshilfe und Frauenheilkunde vol. 49 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	222.	Mosaicism for an additional partial chromosome 8: 46,XX/47,XX+der(8)(p21 leads to qter). [electronic resource] by Pfeiffer, R A Kessel, E Rathgen, E Kulenkampff, M Nehring, T Producer: 19790324 In: Human genetics vol. 44 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	223.	Human Y chromosomes with two fluorescing bands after staining with quinacrine derivates. [electronic resource] by Kim, M A Bier, L Pawlowitzki, I H Pfeiffer, R A Producer: 19720106 In: Humangenetik vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	224.	Studies of malformation syndromes of man XXIV B: the Dubowitz syndrome. Further observations. [electronic resource] by Opitz, J M Pfeiffer, R A Hermann, J P Kushnick, T Producer: 19740308 In: Zeitschrift fur Kinderheilkunde vol. 116 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	225.	Familial reciprocal translocation t(17;19) (q11.2;q13.2) associated with neurofibromatosis type 1, including one patient with non-Hodgkin lymphoma and an additional t(14;20) in B lymphocytes. [electronic resource] by Fahsold, R Habash, T Trautmann, U Haustein, A Pfeiffer, R A Producer: 19950817 In: Human genetics vol. 96 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	226.	[Coloboma and anal atresia: phenotype of a chromosome aberration?]. [electronic resource] by Pfeiffer, R A Heimann, K Heiming, E Schlack, H Maul, H Producer: 19720501 In: Klinische Monatsblatter fur Augenheilkunde vol. 159 Availability: No items available. Save to lists Add to cart (remove)
	227.	Multiple (up to seven) different accessory small marker chromosomes: prenatal diagnosis and follow-up. [electronic resource] by Ulmer, R Pfeiffer, R A Wiest, E Goelz, R Trautmann, U Producer: 19970918 In: Annales de genetique vol. 40 Availability: No items available. Save to lists Add to cart (remove)
	228.	The Zimmermann-Laband syndrome. [electronic resource] by Pfeiffer, R A Seemanova, E Süss, J Müssig, D Tietze, H U Producer: 19920326 In: Klinische Padiatrie vol. 204 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	229.	Identification of a de novo insertional mutation in P0 in a patient with a Déjérine-Sottas syndrome (DSS) phenotype. [electronic resource] by Rautenstrauss, B Nelis, E Grehl, H Pfeiffer, R A Van Broeckhoven, C Producer: 19950228 In: Human molecular genetics vol. 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	230.	Robinow or "fetal face syndrome" in a male infant with ambiguous genitalia and androgen receptor deficiency. [electronic resource] by Schönau, E Pfeiffer, R A Schweikert, H U Böwing, B Schott, G Producer: 19900828 In: European journal of pediatrics vol. 149 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	231.	[Connatal ptosis: a symptom of the syndrome of multiple pterygium and arthrogryposes]. [electronic resource] by Böckel, J Grassl, F Pfeiffer, R A Ruprecht, K W Heidbreder, E Producer: 19841115 In: Klinische Monatsblatter fur Augenheilkunde vol. 185 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	232.	Combination of silver and fluorescent staining for metaphase chromosomes. [electronic resource] by Lau, Y F Pfeiffer, R A Arrighi, F E Hsu, T C Producer: 19780329 In: American journal of human genetics vol. 30 Availability: No items available. Save to lists Add to cart (remove)
	233.	[Acrocephalopolysyndactyly (type II (McKusick) acrocephalosyndactyly or Carpenter's syndrome. Report on 4 cases and an observation of the syndrome of Marshall-Smith (author's transl)]. [electronic resource] by Pfeiffer, R A Seemann, K B Tünte, W Gussone, J Klemm, E Producer: 19770622 In: Klinische Padiatrie vol. 189 Availability: No items available. Save to lists Add to cart (remove)
	234.	[Hypothalamo-hypophyseal dwarfism with inner ear deafness in 2 sisters]. [electronic resource] by Winkelmann, W Solbach, H G Wiegelmann, W Bethge, H Pfeiffer, R A Producer: 19720725 In: Der Internist vol. 13 Availability: No items available. Save to lists Add to cart (remove)
	235.	Nosology of congenital non-progressive cerebellar ataxia. Report on six cases in three families. [electronic resource] by Pfeiffer, R A Palm, D Jünemann, G Mandl-Kramer, S Heimann, E Producer: 19740604 In: Neuropadiatrie vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	236.	[Familial cardiomyopathy with congenital webbed neck]. [electronic resource] by Diekmann, L Pfeiffer, R A Hilgenberg, F Bender, F Reploh, H D Producer: 19681010 In: Munchener medizinische Wochenschrift (1950) vol. 109 Availability: No items available. Save to lists Add to cart (remove)
	237.	Triploid embryo after in vitro fertilization. [electronic resource] by Ulmer, R Rehder, H Trotnow, S Kniewald, A Kniewald, T Pfeiffer, R A Producer: 19860130 In: Archives of gynecology vol. 237 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	238.	[Polysyndactyly, short limbs, and genital malformations--a new syndrome?]. [electronic resource] by Majewski, F Pfeiffer, R A Lenz, W Müller, R Feil, G Seiler, R Producer: 19720217 In: Zeitschrift fur Kinderheilkunde vol. 111 Availability: No items available. Save to lists Add to cart (remove)
	239.	A novel 22q11.2 microdeletion in DiGeorge syndrome. [electronic resource] by Rauch, A Pfeiffer, R A Leipold, G Singer, H Tigges, M Hofbeck, M Producer: 19990413 In: American journal of human genetics vol. 64 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	240.	[Mongolism and leukemia. Clinical and cytogenetic findings in 4 mongoloid children with leukemia]. [electronic resource] by Hellriegel, K P Pfeiffer, R A Seiler, R Schütz, C Rickers, H J Producer: 19691021 In: Munchener medizinische Wochenschrift (1950) vol. 111 Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 274 results.