165 related articles for article (PubMed ID: 6893487)
1. 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]
2. A new syndrome with distinct facial and auricular malformations and dominant inheritance.
Simosa V; Penchaszadeh VB; Bustos T
Am J Med Genet; 1989 Feb; 32(2):184-6. PubMed ID: 2929657
[TBL] [Abstract][Full Text] [Related]
3. Variable expression of rib, pectus, and scapular anomalies with Robin-type cleft palate in a 5-generation family: a new syndrome?
Stalker HJ; Zori RT
Am J Med Genet; 1997 Dec; 73(3):247-50. PubMed ID: 9415678
[TBL] [Abstract][Full Text] [Related]
4. Dandy-Walker(like) malformation, atrio-ventricular septal defect and a similar pattern of minor anomalies in 2 sisters: a new syndrome?
Ritscher D; Schinzel A; Boltshauser E; Briner J; Arbenz U; Sigg P
Am J Med Genet; 1987 Feb; 26(2):481-91. PubMed ID: 3812597
[TBL] [Abstract][Full Text] [Related]
5. Dominant inheritance of syn-camptodactyly of the second and third toes with foot and lower limb asymmetry and scoliosis.
Halal F
Am J Med Genet; 1985 Sep; 22(1):149-56. PubMed ID: 4050850
[TBL] [Abstract][Full Text] [Related]
6. Scoliosis, blindness and arachnodactyly in a large Turkish family: is it a new syndrome?
Dundar M; Erkilic K; Argun M; Caglayan AO; Comeglio P; Koseoglu E; Matyas G; Child AH
Genet Couns; 2008; 19(3):319-30. PubMed ID: 18990988
[TBL] [Abstract][Full Text] [Related]
7. Familial segregation of cervical ribs, Sprengel anomaly, preaxial polydactyly, anal atresia, and urethral obstruction: a new syndrome?
Frydman M; Cohen HA; Ashkenazi A; Varsano I
Am J Med Genet; 1993 Mar; 45(6):717-20. PubMed ID: 8456850
[TBL] [Abstract][Full Text] [Related]
8. VACTERL with hydrocephalus: spontaneous chromosome breakage and rearrangement in a family showing apparent sex-linked recessive inheritance.
Wang H; Hunter AG; Clifford B; McLaughlin M; Thompson D
Am J Med Genet; 1993 Aug; 47(1):114-7. PubMed ID: 8368240
[TBL] [Abstract][Full Text] [Related]
9. Limb pterygium syndromes: a review and report of eleven patients.
Hall JG; Reed SD; Rosenbaum KN; Gershanik J; Chen H; Wilson KM
Am J Med Genet; 1982 Aug; 12(4):377-409. PubMed ID: 7124793
[TBL] [Abstract][Full Text] [Related]
10. New autosomal dominant radial ray hypoplasia syndrome.
Goldblatt J; Viljoen D
Am J Med Genet; 1987 Nov; 28(3):647-54. PubMed ID: 3425633
[TBL] [Abstract][Full Text] [Related]
11. Phenotypic variability in van der Woude syndrome.
Lacombe D; Pedespan JM; Fontan D; Chateil JF; Verloes A
Genet Couns; 1995; 6(3):221-6. PubMed ID: 8588850
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. The G and BBB syndromes: case presentations, genetics, and nosology.
Funderburk SJ; Stewart R
Am J Med Genet; 1978; 2(2):131-44. PubMed ID: 263433
[TBL] [Abstract][Full Text] [Related]
14. [Spondylo-costal dysostosis: presentation of a new case with autosomal dominant heredity and discussion of problems in genetic counseling].
Martello C; Stangoni G; Mezzetti D; Calabro A; Cianfrini D; Lungarotti MS
Pediatr Med Chir; 1992; 14(4):465-8. PubMed ID: 1461791
[TBL] [Abstract][Full Text] [Related]
15. Teebi hypertelorism syndrome.
Koenig R
Clin Dysmorphol; 2003 Jul; 12(3):187-9. PubMed ID: 14564158
[TBL] [Abstract][Full Text] [Related]
16. [Costovertebral dysplasia. A receptor defect of sclerotome development?].
Gassner M
Schweiz Med Wochenschr; 1982 May; 112(22):791-7. PubMed ID: 7100875
[TBL] [Abstract][Full Text] [Related]
17. [Hypo-/aplasia of the nasal bones--an autosomal dominant inherited anomaly].
Ernst M; Schilbach U
HNO; 1987 Nov; 35(11):478-81. PubMed ID: 3692934
[TBL] [Abstract][Full Text] [Related]
18. Vertical transmission of the Ohdo blepharophimosis syndrome.
Mhanni AA; Dawson AJ; Chudley AE
Am J Med Genet; 1998 May; 77(2):144-8. PubMed ID: 9605288
[TBL] [Abstract][Full Text] [Related]
19. Ritscher-Schinzel cranio-cerebello-cardiac (3C) syndrome: report of four new cases and review.
Leonardi ML; Pai GS; Wilkes B; Lebel RR
Am J Med Genet; 2001 Aug; 102(3):237-42. PubMed ID: 11484200
[TBL] [Abstract][Full Text] [Related]
20. VACTERL or MURCS association in a girl with neurenteric cyst and identical thoracic malformations in the father: a case of gonosomal mosaicism?
Orstavik KH; Steen-Johnsen J; Foerster A; Fjeld T; Skullerud K; Lie SO
Am J Med Genet; 1992 Aug; 43(6):1035-8. PubMed ID: 1415331
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]