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	541.	Partial monosomy 3p (3p26.2 --> pter) and partial trisomy 5q (5q34 --> qter) in a girl with coarctation of the aorta, congenital heart defects, short stature, microcephaly and developmental delay. [electronic resource] by Chen, C P Lin, S P Chen, M R Su, Y N Chern, S R Liu, Y P Su, J W Lee, M S Wang, W Producer: 20121120 In: Genetic counseling (Geneva, Switzerland) vol. 23 Availability: No items available. Save to lists Add to cart (remove)
	542.	A three-generation family with terminal microdeletion involving 5p15.33-32 due to a whole-arm 5;15 chromosomal translocation with a steady phenotype of atypical cri du chat syndrome. [electronic resource] by Elmakky, Amira Carli, Diana Lugli, Licia Torelli, Paola Guidi, Battista Falcinelli, Cristina Fini, Sergio Ferrari, Fabrizio Percesepe, Antonio Producer: 20141215 In: European journal of medical genetics vol. 57 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	543.	[Effects of chromosomal aberrations in the pelvic region]. [electronic resource] by Zippel, H Metzke, H Producer: 19720912 In: Padiatrie und Grenzgebiete vol. 11 Availability: No items available. Save to lists Add to cart (remove)
	544.	Clinical and molecular genetic characterization of two siblings with trisomy 2p24.3-pter and monosomy 5p14.3-pter. [electronic resource] by Fukushi, Daisuke Kurosawa, Kenji Suzuki, Yasuyo Suzuki, Kaoru Yamada, Kenichiro Watanabe, Seiji Yokochi, Kenji Wakamatsu, Nobuaki Producer: 20171201 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)
	545.	[Mental retardation in the crying cat syndrome. Comparison of the intellectual level in the partial deletion of the short arm of chromosome 5 with trisomy 21 and deletions of chromosome 18. Apropos of 118 cases taken from the literature]. [electronic resource] by Moor, L Producer: 19681204 In: Revue de neuropsychiatrie infantile et d'hygiene mentale de l'enfance vol. 16 Availability: No items available. Save to lists Add to cart (remove)
	546.	Chromosome disorders in mental retardation. Whose chromosomes to count? [electronic resource] by Schulz, J Producer: 19690220 In: Pediatric clinics of North America vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	547.	Longitudinal development of object permanence in mentally retarded children: an exploratory study. [electronic resource] by Wohlhueter, M J Sindberg, R M Producer: 19750620 In: American journal of mental deficiency vol. 79 Availability: No items available. Save to lists Add to cart (remove)
	548.	A new genomic mechanism leading to cri-du-chat syndrome. [electronic resource] by South, Sarah T Swensen, Jeffrey J Maxwell, Teresa Rope, Alan Brothman, Arthur R Chen, Zhong Producer: 20070125 In: American journal of medical genetics. Part A vol. 140 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	549.	Cri du chat and Potter syndromes: a decision to abort. [electronic resource] by David, A Desai, N Udvardy, M High, D Engelberg, J Producer: 19921015 In: Hospital practice (Office ed.) vol. 27 Availability: No items available. Save to lists Add to cart (remove)
	550.	[Apropos of a translocation of a part of the long arms of a chromosome 5 on the long arms of a chromosome of the D group (Bq-, Dq+)]. [electronic resource] by Beauvais, P Rumpler, Y Ruch, J V Dreyfus, J Haeberle, C Producer: 19690930 In: Archives francaises de pediatrie vol. 26 Availability: No items available. Save to lists Add to cart (remove)
	551.	[Oxygen consumption of leukocytes in chromosome abnormalities. (Down's syndrome, ring chromosome 21, cri-du-chat syndrome, trisomy 18 and 22)]. [electronic resource] by Heyne, K Producer: 19800616 In: Die Medizinische Welt vol. 31 Availability: No items available. Save to lists Add to cart (remove)
	552.	Preimplantation genetic diagnosis of a large pericentric inversion of chromosome 5. [electronic resource] by Iwarsson, E Ahrlund-Richter, L Inzunza, J Rosenlund, B Fridström, M Hillensjö, T Sjöblom, P Nordenskjöld, M Blennow, E Producer: 19981028 In: Molecular human reproduction vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	553.	Problem behaviors associated with deletion Prader-Willi, Smith-Magenis, and cri du chat syndromes. [electronic resource] by Clarke, D J Boer, H Producer: 19990209 In: American journal of mental retardation : AJMR vol. 103 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	554.	MN1-ETV6 fusion gene arising from MDS with 5q-. [electronic resource] by Nofrini, Valeria Berchicci, Laura La Starza, Roberta Gorello, Paolo Di Giacomo, Danika Arcioni, Francesco Pierini, Valentina Crescenzi, Barbara Romoli, Silvia Matteucci, Caterina Mecucci, Cristina Producer: 20110817 In: Leukemia research vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	555.	VACTERL phenotype with mosaic trisomy 5 and uniparental disomy 5. [electronic resource] by Hwang, Samuel Rudd, Mary Katharine Finch, Lisa Peterson, Suzanne E Kapur, Raj P Producer: 20190111 In: American journal of medical genetics. Part A vol. 176 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	556.	[Familial segregation of a t(5p-;13q+). Complementary analysis from specimens preserved in liquid nitrogen]. [electronic resource] by Carpentier, S Dutrillaux, B Lafourcade, J Berger, R Rethoré, M O Lejeune, J Producer: 19720818 In: Annales de genetique vol. 15 Availability: No items available. Save to lists Add to cart (remove)
	557.	Physical mapping of genetic markers on the short arm of chromosome 5. [electronic resource] by Gersh, M Goodart, S A Overhauser, J Producer: 19950518 In: Genomics vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	558.	Comparative mapping of the cri du chat and DiGeorge syndrome regions in the great apes. [electronic resource] by Tarazami, S T Kringstein, A M Conte, R A Verma, R S Producer: 19980925 In: Genes & genetic systems vol. 73 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	559.	A description of adaptive and maladaptive behaviour in children and adolescents with Cri-du-chat syndrome. [electronic resource] by Teixeira, M C T V Emerich, D R Orsati, F T Rimério, R C Gatto, K R Chappaz, I O Kim, C A Producer: 20110610 In: Journal of intellectual disability research : JIDR vol. 55 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	560.	Blood cell galactose-1-phosphate uridyl transferase activity in dysplastic patients, with and without chromosomal aberrations. [electronic resource] by Dahlqvist, A Hall, B Källén, B Producer: 19710204 In: Human heredity vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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