187 related articles for article (PubMed ID: 3425628)
1. New autosomal dominant syndrome resembling craniofrontonasal dysplasia.
Teebi AS
Am J Med Genet; 1987 Nov; 28(3):581-91. PubMed ID: 3425628
[TBL] [Abstract][Full Text] [Related]
2. Delineation of the male phenotype in carniofrontonasal syndrome.
Morris CA; Palumbos JC; Carey JC
Am J Med Genet; 1987 Jul; 27(3):623-31. PubMed ID: 3631134
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Craniofrontonasal dysplasia in a three-generation kindred.
Reynolds JF; Haas RJ; Edgerton MT; Kelly TE
J Craniofac Genet Dev Biol; 1982; 2(3):233-8. PubMed ID: 7166597
[TBL] [Abstract][Full Text] [Related]
5. Autosomal dominant inheritance of the Aarskog syndrome.
Grier RE; Farrington FH; Kendig R; Mamunes P
Am J Med Genet; 1983 May; 15(1):39-46. PubMed ID: 6344635
[TBL] [Abstract][Full Text] [Related]
6. A family with craniofrontonasal dysplasia, and fragile site 12q13 segregating independently.
Kumar D; Clark JW; Blank CE; Patton MA
Clin Genet; 1986 Jun; 29(6):530-7. PubMed ID: 3742859
[TBL] [Abstract][Full Text] [Related]
7. Dominant inheritance of a syndrome similar to Rubinstein-Taybi.
Cotsirilos P; Taylor JC; Matalon R
Am J Med Genet; 1987 Jan; 26(1):85-93. PubMed ID: 3812583
[TBL] [Abstract][Full Text] [Related]
8. Trigonocephaly: a new familial syndrome.
Frydman M; Kauschansky A; Elian E
Am J Med Genet; 1984 May; 18(1):55-9. PubMed ID: 6741996
[TBL] [Abstract][Full Text] [Related]
9. Teebi hypertelorism syndrome.
Koenig R
Clin Dysmorphol; 2003 Jul; 12(3):187-9. PubMed ID: 14564158
[TBL] [Abstract][Full Text] [Related]
10. Polydactyly, conical teeth, nail dysplasia, and short limbs: a new autosomal dominant malformation syndrome.
Curry CJ; Hall BD
Birth Defects Orig Artic Ser; 1979; 15(5B):253-63. PubMed ID: 526581
[No Abstract] [Full Text] [Related]
11. Teebi hypertelorism syndrome (brachycephalofrontonasal dysplasia) in a U.S. family.
Stratton RF
Am J Med Genet; 1991 Apr; 39(1):78-80. PubMed ID: 1867268
[TBL] [Abstract][Full Text] [Related]
12. Cranio-oculo-fronto-nasal malformation: a new MCA condition?
Lopes VL; Campos NL; Maciel-Guerra AT
Clin Dysmorphol; 1997 Jan; 6(1):25-9. PubMed ID: 9018414
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. The nasopalpebral lipoma-coloboma syndrome: a new autosomal dominant dysplasia-malformation syndrome with congenital nasopalpebral lipomas, eyelid colobomas, telecanthus, and maxillary hypoplasia.
Penchaszadeh VB; Velasquez D; Arrivillaga R
Am J Med Genet; 1982 Apr; 11(4):397-410. PubMed ID: 7091184
[TBL] [Abstract][Full Text] [Related]
16. Craniofrontonasal dysplasia: clinical and genetic analysis.
Sax CM; Flannery DB
Clin Genet; 1986 Jun; 29(6):508-15. PubMed ID: 3742856
[TBL] [Abstract][Full Text] [Related]
17. Autosomal dominant inheritance in Setleis syndrome.
Masuno M; Imaizumi K; Makita Y; Nakamura M; Kuroki Y
Am J Med Genet; 1995 May; 57(1):57-60. PubMed ID: 7645599
[TBL] [Abstract][Full Text] [Related]
18. Frontonasal dysplasia: a family presenting autosomal dominant inheritance pattern.
Koçak H; Ceylaner G
Genet Couns; 2009; 20(1):63-8. PubMed ID: 19400543
[TBL] [Abstract][Full Text] [Related]
19. ADULT-syndrome: an autosomal-dominant disorder with pigment anomalies, ectrodactyly, nail dysplasia, and hypodontia.
Propping P; Zerres K
Am J Med Genet; 1993 Mar; 45(5):642-8. PubMed ID: 8456838
[TBL] [Abstract][Full Text] [Related]
20. Syndrome of hydrocephalus, costovertebral dysplasia and Sprengel anomaly with autosomal dominant inheritance.
Waaler PE; Aarskog D
Neuropediatrics; 1980 Aug; 11(3):291-7. PubMed ID: 6893487
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]