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62. A double translocation culture t(5;15)t(9;11) with partial deletion of the short arm of chromosome 5. Repository identification No. GM-344. Jackson L; Barr M; Aronson M; Greene AE; Coriell LL Cytogenet Cell Genet; 1975; 15(6):400-1. PubMed ID: 1225499 [No Abstract] [Full Text] [Related]
63. Short stature and language delay in a 5-year-old girl: 18p- syndrome. Grush ML; Kimberling WJ; Lynch HT Nebr Med J; 1982 Sep; 67(9):261-3. PubMed ID: 7133223 [No Abstract] [Full Text] [Related]
64. Chromosome instability limited to the aneuploid clone in the Pallister-Killian syndrome: a pitfall in prenatal diagnosis. Zollino M; Bajer J; Neri G Prenat Diagn; 1999 Feb; 19(2):184-5. PubMed ID: 10215084 [No Abstract] [Full Text] [Related]
65. Cri du chat syndrome determined by the 5p15.3-->pter deletion--diagnostic problems. Laczmanska I; Stembalska A; Gil J; Czemarmazowicz H; Sasiadek M Eur J Med Genet; 2006; 49(1):87-92. PubMed ID: 16473315 [TBL] [Abstract][Full Text] [Related]
67. Dermatoglyphics in "Cri du Chat" syndrome (5p-). Holt SB; Niebuhr E Birth Defects Orig Artic Ser; 1979; 15(6):565-89. PubMed ID: 552885 [No Abstract] [Full Text] [Related]
68. The Cri du Chat syndrome: epidemiology, cytogenetics, and clinical features. Niebuhr E Hum Genet; 1978 Nov; 44(3):227-75. PubMed ID: 365706 [TBL] [Abstract][Full Text] [Related]
69. [Indications for the examination of chromosomes in ophthalmology]. Vrba M Cesk Oftalmol; 1969 Sep; 25(5):304-6. PubMed ID: 4241557 [No Abstract] [Full Text] [Related]
70. [The importance of configurations or papillary lines in the identification of chromosomal diseases]. Rott HD Folia Clin Int (Barc); 1969 Oct; 19(10):500-6. PubMed ID: 5396731 [No Abstract] [Full Text] [Related]
71. Updating advances in cytogenetics. Applications of the new chromosome banding methods. Breg WR Birth Defects Orig Artic Ser; 1974; 10(8):7-18. PubMed ID: 4142402 [No Abstract] [Full Text] [Related]
72. [Clinical contribution to the crying cat syndrome]. Maaz HJ; Döring M Z Arztl Fortbild (Jena); 1971 Apr; 65(8):439-41. PubMed ID: 5006545 [No Abstract] [Full Text] [Related]
73. [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+)]. Beauvais P; Rumpler Y; Ruch JV; Dreyfus J; Haeberle C Arch Fr Pediatr; 1969; 26(6):695-704. PubMed ID: 5802061 [No Abstract] [Full Text] [Related]
74. Two children with a partial trisomy of chromosome 15 (47,XX, + 15). There appears to be no constellation of physical findings that are characteristic of this abnormality. Parker CE; Mavalwala J; Alfi OS; Weise P; Menon R Clin Pediatr (Phila); 1977 Nov; 16(11):1037-41. PubMed ID: 410577 [No Abstract] [Full Text] [Related]
76. [PARTIAL DELETION OF THE SHORT ARM OF THE 5 CHROMOSOME: THE 5TH CASE OF CRYING CAT SYNDROME]. LEJEUNE J; GAUTIER M; LAFOURCADE J; BERGER R; TURPIN R Ann Genet; 1964; 7():7-10. PubMed ID: 14242109 [No Abstract] [Full Text] [Related]
77. [Identification of 2 familial translocations]. Laurent C; Biemont MC; Robert JM; Dutrillaux B Ann Genet; 1974 Dec; 17(4):279-81. PubMed ID: 4548825 [No Abstract] [Full Text] [Related]
78. Dermatoglyphics in pediatric practice. Kher MB; Indurkar MB; Lokur UV Indian J Med Sci; 1971 Sep; 25(9):618-22. PubMed ID: 4255935 [No Abstract] [Full Text] [Related]
79. An autoradiographic study of the chromosomes in the cri du chat syndrome. Balícek P; Zizka J; Skalská H Sb Ved Pr Lek Fak Karlovy Univerzity Hradci Kralove; 1971; 14(4):405-12. PubMed ID: 5291170 [No Abstract] [Full Text] [Related]
80. Cri du chat-syndrome in combination with partial trisomy 9 p. Sigmund J; Frisch H; Heinz-Erian P; Rhomberg K; Wegner RD Padiatr Padol; 1986; 21(1):61-7. PubMed ID: 3960564 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]