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3. Trisomy 18 with unilateral atypical ectrodactyly. Rogers RC Am J Med Genet; 1994 Jan; 49(1):125-7. PubMed ID: 8172239 [No Abstract] [Full Text] [Related]
4. Unilateral Ectrodactyly in a Newborn with Trisomy 18 Syndrome: An Unusual Association. Kislal FM; Altuntas N; Ozdemir O; Ceylaner S; Kislal MH; Andiran N J Coll Physicians Surg Pak; 2015 Aug; 25(8):619-20. PubMed ID: 26305313 [TBL] [Abstract][Full Text] [Related]
5. Inverted insertion of chromosome 7q and ectrodactyly. Naritomi K; Izumikawa Y; Tohma T; Hirayama K Am J Med Genet; 1993 Jun; 46(5):492-3. PubMed ID: 8322806 [TBL] [Abstract][Full Text] [Related]
6. Monosomy 5p and trisomy 12p in a boy with familial balanced translocation. Vasudevan PC; Parker MJ Clin Dysmorphol; 2006 Apr; 15(2):85-7. PubMed ID: 16531734 [TBL] [Abstract][Full Text] [Related]
7. Ectrodactyly and 7q22.1. Rivera H Am J Med Genet; 1994 Oct; 53(1):89-90. PubMed ID: 7802046 [No Abstract] [Full Text] [Related]
8. Ectrodactyly of hands and feet in a child with a complex translocation including 7q21.2. Sharland M; Patton MA; Hill L Am J Med Genet; 1991 Jun; 39(4):413-4. PubMed ID: 1877619 [TBL] [Abstract][Full Text] [Related]
9. [Diagnosis of Edwards syndrome in newborns]. Dunin-Wasowicz D; Krajewska-Walasek M; Rowecka-Trzebicka K; Gurkau-Malecha M; Gutkowska A; Chrzanowska K Pediatr Pol; 1995 Oct; 70(10):865-74. PubMed ID: 8649934 [TBL] [Abstract][Full Text] [Related]
10. Trisomy 22 and facioauriculovertebral (Goldenhar) sequence. Kobrynski L; Chitayat D; Zahed L; McGregor D; Rochon L; Brownstein S; Vekemans M; Albert DL Am J Med Genet; 1993 Apr; 46(1):68-71. PubMed ID: 8494034 [TBL] [Abstract][Full Text] [Related]
11. [Hereditary transmission of aplasia of the fibula, and of ectrodactyly. Study of a family]. Deragna S; Zucco V; Ferrante E Quad Clin Ostet Ginecol; 1966 Dec; 21(12):1295-308. PubMed ID: 5994965 [No Abstract] [Full Text] [Related]
13. Trisomy 18 syndrome with cleft foot. Castle D; Bernstein R J Med Genet; 1988 Aug; 25(8):568-70. PubMed ID: 3172152 [TBL] [Abstract][Full Text] [Related]
14. Fryns syndrome phenotype and trisomy 22. Ladonne JM; Gaillard D; Carré-Pigeon F; Gabriel R Am J Med Genet; 1996 Jan; 61(1):68-70. PubMed ID: 8741922 [TBL] [Abstract][Full Text] [Related]
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16. Non-mosaic tetrasomy 9p in a liveborn infant with multiple congenital anomalies: case report and comparison with trisomy 9p. Leichtman LG; Zackowski JL; Storto PD; Newlin A Am J Med Genet; 1996 Jun; 63(3):434-7. PubMed ID: 8737648 [TBL] [Abstract][Full Text] [Related]
17. Counseling dilemmas in EEC syndrome. Tekin M; Ohle C; Johnson DE; Christmas JT; Bodurtha J Genet Couns; 2000; 11(1):19-24. PubMed ID: 10756423 [TBL] [Abstract][Full Text] [Related]