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.
9. Metaphyseal dysplasia with maxillary hypoplasia and brachydactyly. Halal F; Picard JL; Raymond-Tremblay D; de Bosset P Am J Med Genet; 1982 Sep; 13(1):71-9. PubMed ID: 7137223 [TBL] [Abstract][Full Text] [Related]
10. [Hemihypertrophy of the body in children]. Labrune B Rev Prat; 1974 Nov 21-Dec 1; 24(53):4821-2 passim. PubMed ID: 4450096 [No Abstract] [Full Text] [Related]
11. MIDAS (microphthalmia, dermal aplasia, sclerocornea) syndrome with central nervous system abnormalities. Carman KB; Yakut A; Sabuncu I; Yarar C Clin Dysmorphol; 2009 Oct; 18(4):234-5. PubMed ID: 19726975 [No Abstract] [Full Text] [Related]
13. Possible examples of the goltz syndrome (focal dermal hypoplasia) without linear areas of skin hypoplasia. Aymé S; Fraser FC Birth Defects Orig Artic Ser; 1982; 18(3B):59-65. PubMed ID: 7139115 [No Abstract] [Full Text] [Related]
14. New syndrome?: MCA/MR syndrome with multiple circumferential skin creases. Elliott AM; Ludman M; Teebi AS Am J Med Genet; 1996 Mar; 62(1):23-5. PubMed ID: 8779319 [TBL] [Abstract][Full Text] [Related]
15. Aniridia and optic nerve hypoplasia. McCulley TJ; Mayer K; Dahr SS; Simpson J; Holland EJ Eye (Lond); 2005 Jul; 19(7):762-4. PubMed ID: 15359227 [TBL] [Abstract][Full Text] [Related]
16. [Familial pelvi-scapulary dysplasia with anomalies of the epiphyses, dwarfism and dysmorphy: a new syndrome? (author's transl)]. Cousin J; Walbaum R; Cegarra P; Huguet J; Louis J; Pauli A; Fournier A; Fontaine G Arch Fr Pediatr; 1982 Mar; 39(3):173-5. PubMed ID: 7103674 [TBL] [Abstract][Full Text] [Related]
17. Clinical manifestations of terminal osseous dysplasia and pigmentary defects in a young girl. Lin BP; Lin MI; Berlocher WC Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 2003 May; 95(5):607-13. PubMed ID: 12738953 [TBL] [Abstract][Full Text] [Related]
18. Partial deletion of chromosome 12q is not usually associated with CFC syndrome. Zollino M; Neri G Am J Med Genet; 2000 Nov; 95(3):296. PubMed ID: 11102944 [No Abstract] [Full Text] [Related]