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	181.	Terminal deletion of the long arm of chromosome 1 in a malformed newborn. [electronic resource] by Kessel, E Pfeiffer, R A Blanke, W Schwarz, J Producer: 19780930 In: Human genetics vol. 42 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	182.	Epiphyseal dysplasia of the femoral head, severe myopia and perceptive hearing loss in three brothers. [electronic resource] by Pfeiffer, R A Jünemann, G Polster, J Bauer, H Producer: 19731113 In: Clinical genetics vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	183.	[On the inheritance of mandibulofaciaal dysostosis]. [electronic resource] by Ammermann, M Pfeiffer, R A Hüther, W Becker, R Producer: 19720309 In: Munchener medizinische Wochenschrift (1950) vol. 113 Availability: No items available. Save to lists Add to cart (remove)
	184.	[Ring chromosomes and centric fragments in Turner's syndrome]. [electronic resource] by Pfeiffer, R A Scharfenberg, W Büchner, T Stolecke, H Producer: 19681006 In: Geburtshilfe und Frauenheilkunde vol. 28 Availability: No items available. Save to lists Add to cart (remove)
	185.	Thalidomide-embryopathy in twins: a collaborative study. [electronic resource] by Jörgensen, G Lenz, W Pfeiffer, R A Schaafhausen, C Producer: 19710415 In: Acta geneticae medicae et gemellologiae vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	186.	Centromeric alphoid DNA heteromorphisms of chromosome 22 revealed by FISH-technique. [electronic resource] by Liehr, T Pfeiffer, R A Trautmann, U Gebhart, E Producer: 19980805 In: Clinical genetics vol. 53 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	187.	[Diagnosis of aneuploidy with fluorescence in situ hybridization (FISH); value in pregnancies with increased risk for chromosome aberrations]. [electronic resource] by Ulmer, R Pfeiffer, R A Kollert, A Beinder, E Producer: 20000419 In: Zeitschrift fur Geburtshilfe und Neonatologie vol. 204 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	188.	[MORPHOLOGY AND DNA-SYNTHESIS OF A RING-CHROMOSOME IN A CHILD WITH TURNER'S SYNDROME]. [electronic resource] by PFEIFFER, R A BUECHNER, T SCHARFENBERG, W SCHLUETER, I Producer: 19961201 In: Klinische Wochenschrift vol. 43 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	189.	[A solitary central maxillary incisor and holoprosencephaly in siblings]. [electronic resource] by Süss, J Pfeiffer, R A Zschiesche, S König, R Producer: 19920528 In: Deutsche zahnarztliche Zeitschrift vol. 45 Availability: No items available. Save to lists Add to cart (remove)
	190.	Beta-glucuronidase deficiency in a girl with unusual clinical features. [electronic resource] by Pfeiffer, R A Kresse, H Bäumer, N Sattinger, E Producer: 19771229 In: European journal of pediatrics vol. 126 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	191.	[Extreme tissue mosaicism in trisomy 8 syndrome. Trisomy 8 in fibroblasts and normal karyotype in lymphocytes]. [electronic resource] by Meisel-Stosiek, M Pfeiffer, R A Tietze, H U Producer: 19831220 In: Klinische Padiatrie vol. 195 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	192.	Deficiency of coagulation factors VII and X associated with deletion of a chromosome 13 (q34). Evidence from two cases with 46,XY,t(13;Y)(q11;q34). [electronic resource] by Pfeiffer, R A Ott, R Gilgenkrantz, S Alexandre, P Producer: 19830527 In: Human genetics vol. 62 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	193.	[Balanced translocation t(15q-;16p+) as cause of habitual abortions]. [electronic resource] by Hasegawa, T Pfeiffer, R A Metz, F Schild, W Producer: 19731116 In: Geburtshilfe und Frauenheilkunde vol. 33 Availability: No items available. Save to lists Add to cart (remove)
	194.	De novo translocation t(Yq-; 15p+) in a malformed boy. [electronic resource] by Pfeiffer, R A Bier, L Majewski, F Rager, K Producer: 19740214 In: Humangenetik vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	195.	Extreme variant of septo-optic dysplasia. [electronic resource] by Stehr, K Mayer, U Pfeiffer, R A Reif, R Producer: 19851226 In: Ophthalmic paediatrics and genetics vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	196.	[Proximal 4p syndrome in a 7-year-old moderately retarded girl]. [electronic resource] by Volleth, M Erhardt, J Schmitzer, E Pfeiffer, R A Producer: 19931021 In: Monatsschrift Kinderheilkunde : Organ der Deutschen Gesellschaft fur Kinderheilkunde vol. 141 Availability: No items available. Save to lists Add to cart (remove)
	197.	Aplasia of the optic nerve in two cases of partial trisomy 10q24-ter. [electronic resource] by Pfeiffer, R A Jünemann, A Lorenz, B Sieber, E Producer: 19960401 In: Clinical genetics vol. 48 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	198.	[Spondylocostal dysostosis. Report of 5 cases including siblings and an atypical case]. [electronic resource] by Pfeiffer, R A Hansen, H G Böwing, B Tietze, U Producer: 19830505 In: Monatsschrift Kinderheilkunde : Organ der Deutschen Gesellschaft fur Kinderheilkunde vol. 131 Availability: No items available. Save to lists Add to cart (remove)
	199.	[Chromosome aberrations in Prader-Willi-Labhart syndrome--critical review, documented by 4 unusual cases]. [electronic resource] by Pfeiffer, R A Tschech, L Irle, U Wündisch, G F Producer: 19880112 In: Klinische Padiatrie vol. 199 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	200.	Prenatal diagnosis of trisomy 9 mosaicism possibly limited to fetal membranes. [electronic resource] by Pfeiffer, R A Ulmer, R Kniewald, A Wagner-Thiessen, E Producer: 19850122 In: Prenatal diagnosis vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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