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.
6. De Novo 17q24.2-q24.3 microdeletion presenting with generalized hypertrichosis terminalis, gingival fibromatous hyperplasia, and distinctive facial features. Afifi HH; Fukai R; Miyake N; Gamal El Din AA; Eid MM; Eid OM; Thomas MM; El-Badry TH; Tosson AM; Abdel-Salam GM; Matsumoto N Am J Med Genet A; 2015 Oct; 167A(10):2418-24. PubMed ID: 26033841 [TBL] [Abstract][Full Text] [Related]
7. Autosomal dominant inheritance in Cantú syndrome (congenital hypertrichosis, osteochondrodysplasia, and cardiomegaly). Lazalde B; Sánchez-Urbina R; Nuño-Arana I; Bitar WE; de Lourdes Ramírez-Dueñas M Am J Med Genet; 2000 Oct; 94(5):421-7. PubMed ID: 11050630 [TBL] [Abstract][Full Text] [Related]
8. A new recessive syndrome of unusual facies and multiple structural abnormalities. Thakker Y; Donnai D J Med Genet; 1991 Sep; 28(9):633-5. PubMed ID: 1956065 [TBL] [Abstract][Full Text] [Related]
9. Syndrome of camptodactyly, multiple ankyloses, facial anomalies and pulmonary hypoplasia--further delineation and evidence for autosomal recessive inheritance. Pena SD; Shokeir MH Birth Defects Orig Artic Ser; 1976; 12(5):201-8. PubMed ID: 953225 [No Abstract] [Full Text] [Related]
10. Hypertrichosis cubiti: two new cases and a review of the literature. Visser R; Beemer FA; Veenhoven RH; De Nef JJ Genet Couns; 2002; 13(4):397-403. PubMed ID: 12558109 [TBL] [Abstract][Full Text] [Related]
11. [Tooth and oral mucosa hereditary anomalies in complex syndromes characterized by hyper- or hypotrichosis]. Giannetti L; Consolo U; Bambini F Minerva Stomatol; 2003; 52(1-2):25-30. PubMed ID: 12686911 [TBL] [Abstract][Full Text] [Related]
12. A new recessive syndrome of unusual facies, digital abnormalities, and ichthyosis. Clayton-Smith J; Donnai D J Med Genet; 1989 May; 26(5):339-42. PubMed ID: 2732996 [TBL] [Abstract][Full Text] [Related]
13. Autosomal recessive versus autosomal dominant inheritance in Larsen syndrome: report of two affected sisters. Knoblauch H; Urban M; Tinschert S Genet Couns; 1999; 10(3):315-20. PubMed ID: 10546105 [TBL] [Abstract][Full Text] [Related]
14. Autosomal dominant inheritance of Barber-Say syndrome. Dinulos MB; Pagon RA Am J Med Genet; 1999 Sep; 86(1):54-6. PubMed ID: 10440829 [TBL] [Abstract][Full Text] [Related]
15. A new syndrome with camptodactyly, joint contractures, facial anomalies, and skeletal defects: a case report and review of syndromes with camptodactyly. Rozin MM; Hertz M; Goodman RM Clin Genet; 1984 Oct; 26(4):342-55. PubMed ID: 6437708 [TBL] [Abstract][Full Text] [Related]
16. Setleis (bitemporal 'forceps marks') syndrome in a German family: evidence for autosomal dominant inheritance. Artlich A; Schwinger E; Meinecke P Clin Dysmorphol; 1992 Jul; 1(3):157-60. PubMed ID: 1342863 [TBL] [Abstract][Full Text] [Related]
17. Three mildly retarded siblings with congenital cataracts, sensorineural deafness, hypogonadism, hypertrichosis and short stature: a new syndrome? Schaap C; Taylor D; Baraitser M Clin Dysmorphol; 1995 Oct; 4(4):283-8. PubMed ID: 8574417 [TBL] [Abstract][Full Text] [Related]
18. What syndrome is this? Gingival fibromatosis-hypertrichosis syndrome. Tay YK; Bellus G; Weston W Pediatr Dermatol; 2001; 18(6):534-6. PubMed ID: 11841646 [No Abstract] [Full Text] [Related]
19. Cone-rod congenital amaurosis associated with congenital hypertrichosis: an autosomal recessive condition. Jalili IK J Med Genet; 1989 Aug; 26(8):504-10. PubMed ID: 2769722 [TBL] [Abstract][Full Text] [Related]
20. Rhombencephalosynapsis with facial anomalies and probable autosomal recessive inheritance: a case report. Romanengo M; Tortori-Donati P; Di Rocco M Clin Genet; 1997 Sep; 52(3):184-6. PubMed ID: 9377810 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]