These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
5. First-trimester diagnosis of familial split-hand/split-foot malformation. Ram KT; Goffman D; Ilagan J; Dar P J Ultrasound Med; 2009 Oct; 28(10):1397-400. PubMed ID: 19778890 [No Abstract] [Full Text] [Related]
6. [Evaluation of infants born to mothers with a history of cocaine use during pregnancy]. Bol Asoc Med P R; 1992 Nov; 84(11):309-11. PubMed ID: 1449571 [No Abstract] [Full Text] [Related]
7. Abnormalities of the hands and feet in the fetus: sonographic findings. Bromley B; Benacerraf B AJR Am J Roentgenol; 1995 Nov; 165(5):1239-43. PubMed ID: 7572511 [TBL] [Abstract][Full Text] [Related]
8. Split hand and foot malformation: ultrasound detection in the first trimester. Lapaire O; Schiesser M; Peukert R; Holzgreve W; Tercanli S Ultrasound Obstet Gynecol; 2002 Nov; 20(5):511-2. PubMed ID: 12423492 [TBL] [Abstract][Full Text] [Related]
9. Microphthalmia and distal limb abnormalities in a child of consanguineous parents. al Gazali LI; Sabarinathan DK; Khidir A Clin Dysmorphol; 1994 Jul; 3(3):258-62. PubMed ID: 7981863 [TBL] [Abstract][Full Text] [Related]
10. First trimester diagnosis of split hand/foot by transvaginal ultrasound. Haak MC; Cobben JM; van Vugt JM Fetal Diagn Ther; 2001; 16(3):146-9. PubMed ID: 11316929 [TBL] [Abstract][Full Text] [Related]
11. Congenital renal abnormalities in infants with in utero cocaine exposure. Rosenstein BJ; Wheeler JS; Heid PL J Urol; 1990 Jul; 144(1):110-2. PubMed ID: 2193169 [TBL] [Abstract][Full Text] [Related]
12. Prenatal diagnosis of a de novo 9p terminal chromosomal deletion in a fetus with major congenital anomalies. Hou WC; Chen CP; Hwang KS; Chen YC; Lai YJ; Tien CY; Su HY Taiwan J Obstet Gynecol; 2014 Dec; 53(4):602-5. PubMed ID: 25510709 [TBL] [Abstract][Full Text] [Related]
13. The possible teratogenic effect of salicylates on the developing fetus. Brief summaries of eight suggestive cases. McNiel JR Clin Pediatr (Phila); 1973 Jun; 12(6):347-50. PubMed ID: 4736229 [No Abstract] [Full Text] [Related]
14. Prenatal diagnosis of Ectrodactyly-Ectodermal dysplasia-Cleft (EEC) syndrome in a Chinese woman with a TP63 mutation. Yang Y; Huang LY; Han J; Li DZ Eur J Obstet Gynecol Reprod Biol; 2017 Jun; 213():146-147. PubMed ID: 28420484 [No Abstract] [Full Text] [Related]
18. Acro-spondylar variant of punctate epiphyseal dysplasia (report of two cases). Kozlowski K; Majewski F Rofo; 1990 Jan; 152(1):115-7. PubMed ID: 2154001 [No Abstract] [Full Text] [Related]
19. Symbrachydactyly involving both the hand and foot. A report of two cases. Uchida T; Kojima T; Hirakawa M; Uchida M Handchir Mikrochir Plast Chir; 1995 Jan; 27(1):51-4. PubMed ID: 7705729 [TBL] [Abstract][Full Text] [Related]
20. Probable identity of Goltz syndrome and Van Allen-Myhre syndrome: evidence from phenotypic evolution. Hancock S; Pryde P; Fong C; Brazy JE; Stewart K; Favour A; Pauli RM Am J Med Genet; 2002 Jul; 110(4):370-9. PubMed ID: 12116212 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]