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	521.	Cri du chat syndrome and complex karyotype in a patient with infantile spasms, hypsarrhythmia, nonketotic hyperglycinemia, and heterotopia. [electronic resource] by Tsao, Chang Y Wenger, Gail D Bartholomew, Dennis W Producer: 20050627 In: American journal of medical genetics. Part A vol. 134A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	522.	Cri-du-chat syndrome combined with partial C-group trisomy. [electronic resource] by Mann, J Rafferty, J H Producer: 19721226 In: Journal of medical genetics vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	523.	A case of monosomy 21 found to be an unbalanced de novo t(5p;21q) by fluorescence in situ hybridization. [electronic resource] by Flaherty, L Moloney, J Watson, N Robson, L Bousfield, L Smith, A Producer: 19981022 In: Journal of intellectual disability research : JIDR vol. 42 ( Pt 3) Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	524.	Anaesthetic considerations for the patient with cri du chat syndrome. [electronic resource] by Brislin, R P Stayer, S A Schwartz, R E Producer: 19960104 In: Paediatric anaesthesia vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	525.	Radiological features of the most common autosomal disorders: trisomy 21-22 (mongolism or Down's syndrome), trisomy 18, trisomy 13-15, and the cri du chat syndrome. [electronic resource] by James, A E Merz, T Janower, M L Dorst, J P Producer: 19720327 In: Clinical radiology vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	526.	Psychomotor development in Cri du Chat Syndrome. [electronic resource] by Cerruti Mainardi, P Guala, A Pastore, G Pozzo, G Dagna Bricarelli, F Pierluigi, M Producer: 20001207 In: Clinical genetics vol. 57 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	527.	[Crying cat syndrome discovered during a routine examination]. [electronic resource] by Lafon, R Emberger, J M Pouget, R Chiariny, J F Producer: 19730319 In: Annales medico-psychologiques vol. 2 Availability: No items available. Save to lists Add to cart (remove)
	528.	Inverted duplication with terminal deletion of 5p and no cat-like cry. [electronic resource] by Wang, Jia-Chi Coe, Bradley P Lomax, Brenda MacLeod, Patrick M Parslow, Malcolm I Schein, Jacqueline E Lam, Wan L Eydoux, Patrice Producer: 20080522 In: American journal of medical genetics. Part A vol. 146A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	529.	Complete maternal isodisomy of chromosome 5 in a Japanese patient with Netherton syndrome. [electronic resource] by Numata, Sanae Hamada, Takahiro Teye, Kwesi Matsuda, Mitsuhiro Ishii, Norito Karashima, Tadashi Kabashima, Kenji Furumura, Minao Ohata, Chika Hashimoto, Takashi Producer: 20140409 In: The Journal of investigative dermatology vol. 134 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	530.	A natural history of a child with monosomy 5p syndrome (Cat-cry/Cri-du-chat syndrome) during the 18 years of follow-up. [electronic resource] by Posmyk, R Panasiuk, B Yatsenko, S A Stankiewicz, P Midro, A T Producer: 20050802 In: Genetic counseling (Geneva, Switzerland) vol. 16 Availability: No items available. Save to lists Add to cart (remove)
	531.	Duplication 5q and deletion 9p due to a t(5;9)(q34;p23) in 2 cousins with features of Hunter-McAlpine syndrome and hypothyroidism. [electronic resource] by Vásquez-Velásquez, A I García-Castillo, H A González-Mercado, M G Dávalos, I P Raca, G Xu, X Dwyer, E Rivera, H Producer: 20110406 In: Cytogenetic and genome research vol. 132 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	532.	Anesthesia in Cri du Chat syndrome: Information on 51 Italian patients. [electronic resource] by Guala, Andrea Spunton, Marianna Mainardi, Paola Cerruti Emmig, Uta Acucella, Gabriela Danesino, Cesare Producer: 20160108 In: American journal of medical genetics. Part A vol. 167A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	533.	Studies on human triosephosphate isomerase. 3. Characterization of the enzyme from patients with the cri du chat syndrome. [electronic resource] by Hendrickson, R J Snapka, R M Sawyer, T H Gracy, R W Producer: 19730912 In: American journal of human genetics vol. 25 Availability: No items available. Save to lists Add to cart (remove)
	534.	Neurological abnormalities in the 'cri-du-chat' syndrome. [electronic resource] by Colover, J Lucas, M Comley, J A Roe, A M Producer: 19730105 In: Journal of neurology, neurosurgery, and psychiatry vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	535.	High-resolution mapping of genotype-phenotype relationships in cri du chat syndrome using array comparative genomic hybridization. [electronic resource] by Zhang, Xiaoxiao Snijders, Antoine Segraves, Richard Zhang, Xiuqing Niebuhr, Anita Albertson, Donna Yang, Huanming Gray, Joe Niebuhr, Erik Bolund, Lars Pinkel, Dan Producer: 20050302 In: American journal of human genetics vol. 76 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	536.	Familial short stature due to a 5q22.1-q23.2 duplication refines the 5q duplication spectrum. [electronic resource] by Zahnleiter, Diana Trautmann, Udo Ekici, Arif B Goehring, Ina Reis, André Dörr, Helmuth-Günther Rauch, Anita Thiel, Christian T Producer: 20111206 In: European journal of medical genetics vol. 54 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	537.	Chromosomal abnormalities in obstetrics and gynecology. [electronic resource] by Krmpotic, E Rosenthal, I M Producer: 19770103 In: Obstetrics and gynecology annual vol. 5 Availability: No items available. Save to lists Add to cart (remove)
	538.	Contrasting age related changes in autism spectrum disorder phenomenology in Cornelia de Lange, Fragile X, and Cri du Chat syndromes: Results from a 2.5 year follow-up. [electronic resource] by Cochran, Lisa Moss, Joanna Nelson, Lisa Oliver, Chris Producer: 20160304 In: American journal of medical genetics. Part C, Seminars in medical genetics vol. 169 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	539.	[Clinical chromosome anomalies (1st part) (author's transl)]. [electronic resource] by Klein, D Producer: 19760409 In: Schweizerische Rundschau fur Medizin Praxis = Revue suisse de medecine Praxis vol. 64 Availability: No items available. Save to lists Add to cart (remove)
	540.	[Modifications of cutaneous elastic fibers in cyring cat disease (apropos of a further case)]. [electronic resource] by Vissian, L Manassero, J Kermarec, J Duplay, H Vaillaud, J C Producer: 19710723 In: Annales de dermatologie et de syphiligraphie vol. 98 Availability: No items available. Save to lists Add to cart (remove)

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