139 related articles for article (PubMed ID: 5410164)
1. Human chromosomal deletion: two patients with the 4p- syndrome.
Arias D; Passarge E; Engle MA; German J
J Pediatr; 1970 Jan; 76(1):82-8. PubMed ID: 5410164
[No Abstract] [Full Text] [Related]
2. Three non-mongoloid patients of similar phenotype with an extra G-like chromosome.
Gustavson KH; Hitrec V; Santesson B
Clin Genet; 1972; 3(2):135-46. PubMed ID: 5054315
[No Abstract] [Full Text] [Related]
3. The 4p-syndrome, with a report of two new cases.
Fryns JP; Eggermont E; Verresen H; Van den Berghe H
Humangenetik; 1973; 19(1):99-109. PubMed ID: 4725911
[No Abstract] [Full Text] [Related]
4. The 4p- syndrome. A clinically recognizable chromosomal deletion syndrome.
Guthrie RD; Aase JM; Asper AC; Smith DW
Am J Dis Child; 1971 Nov; 122(5):421-5. PubMed ID: 5129531
[No Abstract] [Full Text] [Related]
5. New chromosomal syndromes.
Lewandowski RC; Yunis JJ
Am J Dis Child; 1975 Apr; 129(4):515-29. PubMed ID: 124130
[No Abstract] [Full Text] [Related]
6. Partial deletion of the short arm of chromosome no. 4(4p-): clinical studies in five unrelated patients.
Miller OJ; Breg WR; Warburton D; Miller DA; DeCapoa A; Allderdice PW; Davis J; Klinger HP; McGilvray E; Allen FH
J Pediatr; 1970 Nov; 77(5):792-801. PubMed ID: 5504070
[No Abstract] [Full Text] [Related]
7. The short arm deletion syndrome of chromosome 4 (4p- syndrome).
Zellweger H; Bardach J; Bordwell J; Williams K
Arch Otolaryngol; 1975 Jan; 101(1):29-32. PubMed ID: 1119985
[TBL] [Abstract][Full Text] [Related]
8. Inherited pericentric inversion of chromosome no. 4.
Wilson MG; Towner JW; Coffin GS; Forsman I
Am J Hum Genet; 1970 Nov; 22(6):679-90. PubMed ID: 5518460
[No Abstract] [Full Text] [Related]
9. [Cytogenetic and pathological observations in the (4p-) SYNDROME (Wolf syndrome)].
Citoler P; Gropp A; Gullotta F
Beitr Pathol; 1971 Apr; 143(1):84-96. PubMed ID: 5577069
[No Abstract] [Full Text] [Related]
10. Prenatal recognition of 4p- syndrome.
Blunt S; Berry AC; Seller MJ; Williams CA
J Med Genet; 1977 Jun; 14(3):232-3. PubMed ID: 881719
[TBL] [Abstract][Full Text] [Related]
11. Identification of 21r and 22r chromosomes by quinacrine fluorescence.
Crandall BF; Weber F; Muller HM; Burwell JK
Clin Genet; 1972; 3(4):264-70. PubMed ID: 5054320
[No Abstract] [Full Text] [Related]
12. Interstitial deletion of the short arm of chromosome 4.
Ray M; Evans J; Rockman-Greenberg C; Wickstrom D
J Med Genet; 1984 Jun; 21(3):223-5. PubMed ID: 6748021
[TBL] [Abstract][Full Text] [Related]
13. 4p- phenotype in an infant with t(4p-;19p or q+)mat translocation.
Neu RL; Shott RJ; Gardner LI
Am J Dis Child; 1975 Mar; 129(3):363-5. PubMed ID: 1121967
[TBL] [Abstract][Full Text] [Related]
14. Deletion from the long arm of chromosome 4 (46,XX,4q-) associated with congenital anomalies.
Golbus MS; Conte FA; Daentl DL
J Med Genet; 1973 Mar; 10(1):83-5. PubMed ID: 4121427
[TBL] [Abstract][Full Text] [Related]
15. New syndrome associated with partial deletion of short arms of chromosome No. 4. Clinical manifestations of hypospadias, beaked nose, abnormal iris, hemangioma of forehead, seizures, and other anomalies.
Leão JC; Bargman GJ; Neu RL; Kajii T; Gardner LI
JAMA; 1967 Oct; 202(5):434-7. PubMed ID: 6072506
[No Abstract] [Full Text] [Related]
16. 4p- syndrome and 9p tetrasomy mosaicism with cleft lip and palate.
Kobayashi J; Kimijima Y; Yamada S; Amagasa T; Saito-Ohara F
J Craniomaxillofac Surg; 2000 Jun; 28(3):165-70. PubMed ID: 10964553
[TBL] [Abstract][Full Text] [Related]
17. Trisomy 13 syndrome in Chinese infants. Clinical findings and incidence.
Yu FC; Gutman LT; Huang SW; Fresh JW; Emanuel I
J Med Genet; 1970 Jun; 7(2):132-7. PubMed ID: 5519598
[No Abstract] [Full Text] [Related]
18. Ring-G chromosome, a new G-deletion syndrome?
Weleber RG; Hecht F; Giblett ER
Am J Dis Child; 1968 Apr; 115(4):489-93. PubMed ID: 4296014
[No Abstract] [Full Text] [Related]
19. Retinoblastoma and deletion D (14) syndrome.
Wilson MG; Melnyk J; Towner JW
J Med Genet; 1969 Sep; 6(3):322-7. PubMed ID: 5345106
[No Abstract] [Full Text] [Related]
20. Computer-assisted analysis of chromosomal abnormalities: detection of a deletion in aniridia-Wilms' tumor syndrome.
Ladda R; Atkins L; Littlefield J; Neurath P; Marimuthu KM
Science; 1974 Aug; 185(4153):784-7. PubMed ID: 4367262
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]