124 related articles for article (PubMed ID: 1320183)
1. [Maxillofacial and dental abnormalities in some multiple abnormality syndromes. "Cri du chat" syndrome, Wilms' tumor-aniridia syndrome; Sotos syndrome; Goldenhar syndrome].
Berio A; Trucchi R; Meliota M
Minerva Pediatr; 1992 May; 44(5):223-9. PubMed ID: 1320183
[TBL] [Abstract][Full Text] [Related]
2. Aniridia-Wilms' tumour syndrome--a case report.
Vidyasagar MS; Sagar SV; Kumar GR; Rao P
Indian J Ophthalmol; 1992; 40(4):122-3. PubMed ID: 1338631
[TBL] [Abstract][Full Text] [Related]
3. [Maxillofacial and dental anomalies in multiple-abnormality syndromes. The clinical and therapeutic aspects in Sotos' syndrome].
Staffolani N; Belcastro S; Guerra M
Minerva Stomatol; 1994 Nov; 43(11):525-9. PubMed ID: 7739485
[TBL] [Abstract][Full Text] [Related]
4. [Cri-du-chat syndrome and two other deformed children in a family carrying a pericentric inversion or insertion of chromosome 5].
Delozier-Blanchet CD; Pitmon D; Schorderet D; Engel E
J Genet Hum; 1985 Dec; 33(5):371-80. PubMed ID: 4093767
[TBL] [Abstract][Full Text] [Related]
5. The Perlman syndrome: familial renal dysplasia with Wilms tumor, fetal gigantism and multiple congenital anomalies.
Neri G; Martini-Neri ME; Katz BE; Opitz JM
Am J Med Genet; 1984 Sep; 19(1):195-207. PubMed ID: 6093533
[TBL] [Abstract][Full Text] [Related]
6. The "cri du chat" syndrome.
Mladkovskaya TB; Lebedev BV; Mazaeva IV
Sov Genet; 1970 Oct; 6(10):1374-9. PubMed ID: 4272596
[No Abstract] [Full Text] [Related]
7. [Extraocular changes in congenital aniridia].
Odehnal M; Brůnová B; Krásný J
Cesk Oftalmol; 1992 Mar; 48(2):99-103. PubMed ID: 1326417
[TBL] [Abstract][Full Text] [Related]
8. Cri-du-chat syndrome in a 10 year old girl with deletion of the short arms of chromosome number 5. Observations on dermatoglyphics, maxillo-mandibular measurements and sound spectrograms.
Schlegel RJ; Neu RL; Carneiro Leão J; Reiss JA; Nolan TB; Gardner LI
Helv Paediatr Acta; 1967 Apr; 22(1):2-12. PubMed ID: 5585047
[No Abstract] [Full Text] [Related]
9. Cri du chat and Potter syndromes: a decision to abort.
David A; Desai N; Udvardy M; High D; Engelberg J
Hosp Pract (Off Ed); 1992 Sep; 27(9):197-200, 204-6. PubMed ID: 1522159
[No Abstract] [Full Text] [Related]
10. 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]
11. Assessment of orofacial characteristics and oral pathology associated with cri-du-chat syndrome.
Rodríguez-Caballero A; Torres-Lagares D; Yáñez-Vico RM; Gutiérrez-Pérez JL; Machuca-Portillo G
Oral Dis; 2012 Mar; 18(2):191-7. PubMed ID: 22035137
[TBL] [Abstract][Full Text] [Related]
12. [Newly discovered structural chromosome aberrations in long familial syndromes, associations and sequences. Prader-Willi syndrome, Miller-Dieker syndrome, Giedion-Langer syndrome, Aniridia-Wilms' tumor association, DiGeorge sequence, Wiedemann-Beckwith syndrome].
Schinzel A
Ergeb Inn Med Kinderheilkd; 1988; 57():57-75. PubMed ID: 2850909
[No Abstract] [Full Text] [Related]
13. Goldenhar and cri-du-chat syndromes: a contiguous gene deletion syndrome?
Choong YF; Watts P; Little E; Beck L
J AAPOS; 2003 Jun; 7(3):226-7. PubMed ID: 12825068
[TBL] [Abstract][Full Text] [Related]
14. Goldenhar's syndrome associated with multiple congenital abnormalities.
Bayraktar S; Bayraktar ST; Ataoglu E; Ayaz A; Elevli M
J Trop Pediatr; 2005 Dec; 51(6):377-9. PubMed ID: 16186139
[TBL] [Abstract][Full Text] [Related]
15. [Cri-du-chat syndrome. A case report].
Diop IB; Sy Signate H; Ba SA; Sarr M; Hane L; Diame H; Kane A; Dieye O; Sow D; Diouf SM; Fall M
Dakar Med; 2000; 45(1):95-7. PubMed ID: 14666800
[TBL] [Abstract][Full Text] [Related]
16. [Partial deletion of the short arm of chromosome 4 (Wolf's syndrome). Two further cases].
Schinzel A; Schmid W
Arch Genet (Zur); 1972; 45(2):88-98. PubMed ID: 4657590
[No Abstract] [Full Text] [Related]
17. [The ri-du-chat syndrome].
Krauze M; Marszał E; Siemianowicz S; Helis W; Marek J
Wiad Lek; 1984 Apr; 37(8):640-3. PubMed ID: 6495740
[No Abstract] [Full Text] [Related]
18. [Wilms' tumor and aniridia--a genetically determined syndrome?].
Neidhardt M
Klin Padiatr; 1972 Jul; 184(4):312-7. PubMed ID: 4404179
[No Abstract] [Full Text] [Related]
19. Cri du chat mosaicism: an unusual case of partial deletion and partial deletion/ duplication of the short arm of chromosome 5, leading to an unusual cri du chat phenotype.
Murru D; Boccone L; Ristaldi MS; Nucaro AL
Genet Couns; 2008; 19(4):381-6. PubMed ID: 19239081
[TBL] [Abstract][Full Text] [Related]
20. Supernumerary teeth and dental management in Sotos syndrome.
Raitz R; Laragnoit A
J Dent Child (Chic); 2009; 76(3):246-50. PubMed ID: 19941770
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
