80 related articles for article (PubMed ID: 3189403)
21. Another family with tricho-rhino-phalangeal syndrome type III (Sugio-Kajii syndrome).
Nagai T; Nishimura G; Kasai H; Hasegawa T; Kato R; Ohashi H; Fukushima Y
Am J Med Genet; 1994 Feb; 49(3):278-80. PubMed ID: 8209886
[TBL] [Abstract][Full Text] [Related]
22. Craniofrontonasal dysplasia: more severe expression in the mother than in her son.
Devriendt K; Van Mol C; Fryns JP
Genet Couns; 1995; 6(4):361-4. PubMed ID: 8775424
[TBL] [Abstract][Full Text] [Related]
23. Acalvaria and occipital scalp defects.
Fryns JP
Am J Med Genet; 1994 Feb; 49(3):361. PubMed ID: 8209904
[No Abstract] [Full Text] [Related]
24. [Trichorhinophalangeal syndrome : analysis of craniofacial architecture in six cases (author's transl)].
Scheffer P; Verdier M; Finidori G
Rev Stomatol Chir Maxillofac; 1981; 82(4):230-3. PubMed ID: 6944759
[TBL] [Abstract][Full Text] [Related]
25. Tricho-dento-osseous syndrome: heterogeneity or clinical variability.
Shapiro SD; Quattromani FL; Jorgenson RJ; Young RS
Am J Med Genet; 1983 Oct; 16(2):225-36. PubMed ID: 6650567
[TBL] [Abstract][Full Text] [Related]
26. Ruvalcaba syndrome: autosomal dominant inheritance.
Sugio Y; Kajii T
Am J Med Genet; 1984 Dec; 19(4):741-53. PubMed ID: 6517098
[TBL] [Abstract][Full Text] [Related]
27. Teebi hypertelorism syndrome.
Koenig R
Clin Dysmorphol; 2003 Jul; 12(3):187-9. PubMed ID: 14564158
[TBL] [Abstract][Full Text] [Related]
28. Further evidence of dominant inheritance of Kabuki syndrome.
Pottinger CC; Stiff RE; Holroyd JM; Davies SJ
Clin Dysmorphol; 2009 Oct; 18(4):215-7. PubMed ID: 19625956
[No Abstract] [Full Text] [Related]
29. Does the cranio-cerebello-cardiac syndrome (3C syndrome) include abdominal malformations?
Mégarbané A; Haddad J
Clin Dysmorphol; 1999 Oct; 8(4):305-7. PubMed ID: 10532184
[TBL] [Abstract][Full Text] [Related]
30. Inheritance of Niikawa-Kuroki (Kabuki makeup) syndrome.
Silengo M; Lerone M; Seri M; Romeo G
Am J Med Genet; 1996 Dec; 66(3):368. PubMed ID: 8985504
[No Abstract] [Full Text] [Related]
31. Possibly new multiple congenital anomaly syndrome: cranio-fronto-nasal dysplasia with Poland anomaly.
Erdoğan B; Aköz T; Görgü M; Kutlay R; Dağ F
Am J Med Genet; 1996 Oct; 65(3):222-5. PubMed ID: 9240748
[TBL] [Abstract][Full Text] [Related]
32. Dominant inheritance of microcephaly, short stature and congenital dislocation of the hips.
Newbury-Ecob RA; Young ID
Clin Dysmorphol; 1993 Jan; 2(1):34-8. PubMed ID: 8298736
[TBL] [Abstract][Full Text] [Related]
33. Dominant inheritance of Kabuki make-up syndrome.
Tsukahara M; Kuroki Y; Imaizumi K; Miyazawa Y; Matsuo K
Am J Med Genet; 1997 Nov; 73(1):19-23. PubMed ID: 9375917
[TBL] [Abstract][Full Text] [Related]
34. The Greig cephalopolysyndactyly syndrome: report of a family and review of the literature.
Gollop TR; Fontes LR
Am J Med Genet; 1985 Sep; 22(1):59-68. PubMed ID: 3901752
[TBL] [Abstract][Full Text] [Related]
35. [Acceleration of bone maturation and dysmorphic syndrome in 2 siblings (Marshall-Weaver syndrome)].
Jalaguier J; Montoya F; Germain M; Bonnet H
J Genet Hum; 1983 Dec; 31 Suppl 5():385-95. PubMed ID: 6674414
[TBL] [Abstract][Full Text] [Related]
36. 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]
37. Toriello-Carey syndrome: report of a new case.
Camera G; Righi E; Romagnoli G
Clin Dysmorphol; 1993 Jul; 2(3):260-3. PubMed ID: 7506967
[TBL] [Abstract][Full Text] [Related]
38. [A Swiss family with Klein-Waardenburg's syndrome associated with hyperkeratosis of the palms and feet and with serious oligophrenia].
Amini-Elihou S
J Genet Hum; 1970 Dec; 18(4):307-63. PubMed ID: 5524816
[No Abstract] [Full Text] [Related]
39. [Cranio-mandibular embryology and genetics].
Vanbesien Y
Orthod Fr; 1978; 49():13-9. PubMed ID: 289938
[No Abstract] [Full Text] [Related]
40. 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]
[Previous] [Next] [New Search]
