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	341.	Bilateral radial agenesis with absent thumbs, complex heart defect, short stature, and facial dysmorphism in a patient with pure distal microduplication of 5q35.2-5q35.3. [electronic resource] by Jamsheer, Aleksander Sowińska, Anna Simon, Dorota Jamsheer-Bratkowska, Małgorzata Trzeciak, Tomasz Latos-Bieleńska, Anna Producer: 20130404 In: BMC medical genetics vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	342.	A prenatal diagnosis of mosaic trisomy 5 reveals a postnatal complete uniparental disomy of chromosome 5 with multiple congenital anomalies. [electronic resource] by Reittinger, Andrew M Helm, Benjamin M Boles, Debra J Gadi, Inder K Schrier Vergano, Samantha A Producer: 20171130 In: American journal of medical genetics. Part A vol. 173 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	343.	[Diseases of the larynx in children. Current questions]. [electronic resource] by Muler, H Producer: 19671219 In: Problemes actuels d'oto-rhino-laryngologie p. 307-20 Availability: No items available. Save to lists Add to cart (remove)
	344.	Deletion of the telomerase reverse transcriptase gene and haploinsufficiency of telomere maintenance in Cri du chat syndrome. [electronic resource] by Zhang, Anju Zheng, Chengyun Hou, Mi Lindvall, Charlotta Li, Ke-Jun Erlandsson, Fredrik Björkholm, Magnus Gruber, Astrid Blennow, Elisabeth Xu, Dawei Producer: 20030505 In: American journal of human genetics vol. 72 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	345.	Dandy-Walker syndrome and corpus callosum agenesis in 5p deletion. [electronic resource] by Vialard, F Robyr, R Hillion, Y Molina Gomes, D Selva, J Ville, Y Producer: 20050726 In: Prenatal diagnosis vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	346.	Clinical delineation of a patient with trisomy 1q32.qter and monosomy 5p resulting from a familial translocation 1;5. [electronic resource] by Flores Ramírez, F Abreu González, M García Delgado, C Aparicio Onofre, A Guevara Yáñez, R Sánchez Urbina, R Murguía Peniche, T Ramírez-Ortíz, M A Ibarra Ríos, D Ortiz de Luna, R I Cervantes Peredo, A B Morán Barroso, V F Producer: 20110302 In: Genetic counseling (Geneva, Switzerland) vol. 21 Availability: No items available. Save to lists Add to cart (remove)
	347.	[Cytogenetic and molecular genetic diagnosis of a neonate with partial 13q trisomy and partial 5p monosomy]. [electronic resource] by Xiao, Wenjun Gao, Zhenkui Meng, Qian Zhang, Man Producer: 20150324 In: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics vol. 31 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	348.	Consonant production and intelligibility in cri du chat syndrome. [electronic resource] by Kristoffersen, Kristian E Garmann, Nina Gram Simonsen, Hanne Gram Producer: 20151006 In: Clinical linguistics & phonetics vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	349.	Metabolic anomalies in cri du chat syndrome (5p-) lymphocytes and de novo purine synthesis. [electronic resource] by Peeters, M A Rethoré, M O Aris, L Megarbane, A Cattaneo, F Lejeune, J Producer: 19920521 In: Annales de genetique vol. 34 Availability: No items available. Save to lists Add to cart (remove)
	350.	A Y/5 translocation in a 45,X male with cri du chat syndrome. [electronic resource] by Weber, B Schempp, W Orth, U Seidel, H Gal, A Producer: 19871117 In: Human genetics vol. 77 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	351.	[Cri-du-chat syndrome and two other deformed children in a family carrying a pericentric inversion or insertion of chromosome 5]. [electronic resource] by Delozier-Blanchet, C D Pitmon, D Schorderet, D Engel, E Producer: 19860331 In: Journal de genetique humaine vol. 33 Availability: No items available. Save to lists Add to cart (remove)
	352.	Cri du chat syndrome [46, XY, 5p-] with balanced B/F translocation in father and grandfather: a case report. [electronic resource] by Char, F Producer: 19750909 In: Birth defects original article series vol. 10 Availability: No items available. Save to lists Add to cart (remove)
	353.	Cri-du-chat syndrome diagnosed by amniocentesis performed due to abnormal maternal serum test. [electronic resource] by Fankhauser, L Brundler, A M Dahoun, S Producer: 19990128 In: Prenatal diagnosis vol. 18 Availability: No items available. Save to lists Add to cart (remove)
	354.	Correlation between ultrasound and pathological examination in a prenatal diagnosis of Cri du Chat syndrome associated with partial trisomy 17q. [electronic resource] by Cordier, A G Braidy, C Levaillant, J M Brisset, S Maurin, M L Mas, A E Frydman, R Tachdjian, G Picone, O Producer: 20081104 In: Prenatal diagnosis vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	355.	Breakpoint delineation in 5p- patients leads to new insights about microcephaly and the typical high-pitched cry. [electronic resource] by Chehimi, Samar N Zanardo, Évelin A Ceroni, José R M Nascimento, Amom M Madia, Fabrícia A R Dias, Alexandre T Filho, Gil M N Montenegro, Marília M Damasceno, Jullian Costa, Thaís V M M Gasparini, Yanca Kim, Chong A Kulikowski, Leslie D Producer: 20210326 In: Molecular genetics & genomic medicine vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	356.	Cytologic observations in 35 individuals with a 5p- karyotype. [electronic resource] by Niebuhr, E Producer: 19780915 In: Human genetics vol. 42 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	357.	[Prenatal diagnoses in a family with pericentric inversion of chromosome no. 5]. [electronic resource] by Körner, H Degen, B Röse, I Metschkarski, S Producer: 19831123 In: Zentralblatt fur Gynakologie vol. 105 Availability: No items available. Save to lists Add to cart (remove)
	358.	[General observations on human constitutional diseases caused by autosome aberrations]. [electronic resource] by Lafourcade, J Producer: 19690326 In: Minerva pediatrica vol. 19 Availability: No items available. Save to lists Add to cart (remove)
	359.	A survey of the prevalence of stereotypy, self-injury and aggression in children and young adults with Cri du Chat syndrome. [electronic resource] by Collins, M S Ross Cornish, K Producer: 20020605 In: Journal of intellectual disability research : JIDR vol. 46 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	360.	Early play behaviour in children with 5p- (Cri-du-Chat) syndrome. [electronic resource] by Sarimski, K Producer: 20030618 In: Journal of intellectual disability research : JIDR vol. 47 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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