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7. Townes-Brocks syndrome in an infant with translocation t (5;16). Serville F; Lacombe D; Saura R; Billeaud C; Sergent MP Genet Couns; 1993; 4(2):109-12. PubMed ID: 8357560 [TBL] [Abstract][Full Text] [Related]
8. Inverted duplication of 22pter----q11.21 in cat-eye syndrome. Hoo JJ; Robertson A; Fowlow SB; Bowen P; Lin CC Am J Med Genet; 1986 Jul; 24(3):543-5. PubMed ID: 3728573 [No Abstract] [Full Text] [Related]
9. The dup(3)(p25 leads to pter) syndrome: a case with holoprosencephaly. Martin NJ; Steinberg BG Am J Med Genet; 1983 Apr; 14(4):767-72. PubMed ID: 6846406 [TBL] [Abstract][Full Text] [Related]
10. Recognizable patterns of human malformation. Smith DW Major Probl Clin Pediatr; 1976; 7():1-497. PubMed ID: 940360 [No Abstract] [Full Text] [Related]
11. Pallister-Killian syndrome: a report of 2 cases and review of its surgical aspects. Baglaj M; King J; Carachi R J Pediatr Surg; 2008 Jun; 43(6):1218-21. PubMed ID: 18558213 [TBL] [Abstract][Full Text] [Related]
12. Further delineation of the dup(3q) syndrome. Wilson GN; Dasouki M; Barr M Am J Med Genet; 1985 Sep; 22(1):117-23. PubMed ID: 4050847 [TBL] [Abstract][Full Text] [Related]
13. Cat-eye syndrome: evaluation of the extra chromosome with banding techniques. Case report. De Chieri R; Malfatti C; Stanchi F; Albores JM J Genet Hum; 1974 Jun; 22(2):101-7. PubMed ID: 4213897 [No Abstract] [Full Text] [Related]
14. [A case of multiple congenital anomalies with familial C-G translocation]. Yanagisawa S; Adachi K Jinrui Idengaku Zasshi; 1970 Mar; 14(4):309-15. PubMed ID: 5464693 [No Abstract] [Full Text] [Related]
15. [Monosomy C with mosaicism and thymic dysplasia]. Bigliocchi A; Mattioli P; Ciarla MV; Madonna V Pediatria (Napoli); 1976 Jun; 84(2):307-19. PubMed ID: 1018997 [No Abstract] [Full Text] [Related]
16. [Extra mini-chromosome with symptoms of cat-eye syndrome]. Méhes K; Bajnóczky K; Schmidt P Orv Hetil; 1985 Apr; 126(17):1037-9. PubMed ID: 3991187 [No Abstract] [Full Text] [Related]
17. A case of Aarskog syndrome with a review of Japanese literature. Aihara K; Nishi Y; Usui T Hiroshima J Med Sci; 1982 Jun; 31(2):87-90. PubMed ID: 7129954 [No Abstract] [Full Text] [Related]
19. Familial segregation of cervical ribs, Sprengel anomaly, preaxial polydactyly, anal atresia, and urethral obstruction: a new syndrome? Frydman M; Cohen HA; Ashkenazi A; Varsano I Am J Med Genet; 1993 Mar; 45(6):717-20. PubMed ID: 8456850 [TBL] [Abstract][Full Text] [Related]