127 related articles for article (PubMed ID: 9375917)
21. 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]
22. [Kabuki make-up syndrome].
Kuroki Y
Ryoikibetsu Shokogun Shirizu; 2000; (30 Pt 5):272-3. PubMed ID: 11057225
[No Abstract] [Full Text] [Related]
23. [Special anesthesiological aspects in patients with Niikawa-Kuroki ("Kabuki Make-Up") syndrome].
Wappler F; Standl T
Anasthesiol Intensivmed Notfallmed Schmerzther; 1997 Mar; 32(3):197-200. PubMed ID: 9190168
[TBL] [Abstract][Full Text] [Related]
24. The Williams syndrome: evidence for possible autosomal dominant inheritance.
Sadler LS; Robinson LK; Verdaasdonk KR; Gingell R
Am J Med Genet; 1993 Sep; 47(4):468-70. PubMed ID: 8256806
[TBL] [Abstract][Full Text] [Related]
25. Cataracts, motor system disorder, short stature, learning difficulties, and skeletal abnormalities: a new syndrome?
Slavotinek AM; Pike M; Mills K; Hurst JA
Am J Med Genet; 1996 Mar; 62(1):42-7. PubMed ID: 8779323
[TBL] [Abstract][Full Text] [Related]
26. [Kabuki syndrome].
Stankovics J
Orv Hetil; 1995 Aug; 136(34):1841-3. PubMed ID: 7651720
[TBL] [Abstract][Full Text] [Related]
27. Autosomal dominant Russell-Silver syndrome.
Al-Fifi S; Teebi AS; Shevell M
Am J Med Genet; 1996 Jan; 61(1):96-7. PubMed ID: 8741931
[No Abstract] [Full Text] [Related]
28. A three generations family with blepharo-naso-facial malformations suggestive of Pashayan syndrome.
Stoll C; Terzic J; Fischbach M
Genet Couns; 1999; 10(4):337-43. PubMed ID: 10631920
[TBL] [Abstract][Full Text] [Related]
29. Report of two cases with Van der Woude syndrome: a child and her mother.
Koçer U; Aksoy HM; Tiftikcioğlu YO; Cöloğlu H; Karaaslan O
Genet Couns; 2001; 12(4):341-6. PubMed ID: 11837602
[TBL] [Abstract][Full Text] [Related]
30. Teebi hypertelorism syndrome: report of a third family.
Toriello HV; Delp K
Clin Dysmorphol; 1994 Oct; 3(4):335-9. PubMed ID: 7894738
[TBL] [Abstract][Full Text] [Related]
31. Anorectal anomalies, diaphragmatic defect, cleft palate, lower lip pits, hypopigmentation and hypogammaglobulinemia A in Kabuki syndrome: a rare combination.
Abdel-Salam GM; Afifi HH; Eid MM; el-Badry TH; Kholoussi NM
Genet Couns; 2008; 19(3):309-17. PubMed ID: 18990987
[TBL] [Abstract][Full Text] [Related]
32. Split hand/split foot, syndactyly, urinary tract obstruction, radial, diaphragmatic, and neural tube defects: Czeizel-Losonci syndrome?
Genuardi M; Silvestri E; Tozzi C
Am J Med Genet; 1994 Jul; 51(3):247-50. PubMed ID: 8074153
[TBL] [Abstract][Full Text] [Related]
33. Kabuki syndrome and trisomy 10p.
Utine GE; Alanay Y; Atkaş D; Boduroğlu K; Alikaşifoğlu M; Tunçbilek E
Genet Couns; 2008; 19(3):291-300. PubMed ID: 18990985
[TBL] [Abstract][Full Text] [Related]
34. [Kabuki syndrome, a congenital syndrome with multiple anomalies].
den Biggelaar AM; Kuijpers-Jagtman AM; Bergé SJ; Katsaros C
Ned Tijdschr Tandheelkd; 2006 Dec; 113(12):516-9. PubMed ID: 17193989
[TBL] [Abstract][Full Text] [Related]
35. Congenital hypoplastic anaemia in a patient with a new multiple congenital anomalies-mental retardation syndrome.
Mori PG; Priolo M; Lerone M; Pasino M; Caroli F; Cusano R; Seri M; Silengo MC
Am J Med Genet; 1999 Nov; 87(1):36-9. PubMed ID: 10528244
[TBL] [Abstract][Full Text] [Related]
36. Anesthesia management in Kabuki make-up syndrome.
Sivaci R; Kahveci OK; Celik M; Altuntas A; Solak M
Saudi Med J; 2005 Dec; 26(12):1980-2. PubMed ID: 16380786
[TBL] [Abstract][Full Text] [Related]
37. Oculo-dento-digital dysplasia (OMIM *164200). Full manifestation of the syndrome in a 9.5 year-old girl and type III syndactyly in the father.
Ioan DM; Dagomiz D; Fryns JP
Genet Couns; 2002; 13(2):187-9. PubMed ID: 12150221
[TBL] [Abstract][Full Text] [Related]
38. Prophylactic Oophorectomy: Reducing the U.S. Death Rate from Epithelial Ovarian Cancer. A Continuing Debate.
Piver MS
Oncologist; 1996; 1(5):326-330. PubMed ID: 10388011
[TBL] [Abstract][Full Text] [Related]
39. Schilbach-Rott syndrome in a third family: further delineation of an autosomal dominant trait.
Becerra-Solano LE; Casillas-Avila MP; Díaz-Rodríguez M; Nastasi-Catanese JA; Toscano-Flores JJ; Ramírez-Dueñas ML
Genet Couns; 2007; 18(3):317-23. PubMed ID: 18019373
[TBL] [Abstract][Full Text] [Related]
40. Dominant syndrome with isolated cryptophthalmos and ocular anomalies.
Saal HM; Traboulsi EI; Gavaris P; Samango-Sprouse CA; Parks M
Am J Med Genet; 1992 Jul; 43(5):785-8. PubMed ID: 1642262
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
