101 related articles for article (PubMed ID: 4798674)
1. [A new syndrome caused by deletion of a part of a chromosome (13 q-). Case descriptions and compilation of symptoms (author's transl)].
Grosse KP; Schwanitz G
Klin Padiatr; 1973 Nov; 185(6):468-73. PubMed ID: 4798674
[No Abstract] [Full Text] [Related]
2. [18 q deletion in mother and daughter (author's transl)].
Sulzer M; Zierler H
Wien Klin Wochenschr; 1976 Sep; 88(17):571-5. PubMed ID: 997544
[TBL] [Abstract][Full Text] [Related]
3. Deletion of the short arm of chromosome no.9 (46,9p-): a new deletion syndrome.
Alfi O; Donnell GN; Crandall BF; Derencsenyi A; Menon R
Ann Genet; 1973 Mar; 16(1):17-22. PubMed ID: 4541805
[No Abstract] [Full Text] [Related]
4. [Ring chromosome 13 and multiple malformations (author's transl)].
Antich J; Plaza J; Geán E
An Esp Pediatr; 1981 Nov; 15(5):469-73. PubMed ID: 7332149
[TBL] [Abstract][Full Text] [Related]
5. Familial 18 q- syndrome.
Law EM; Masterson JG
Ann Genet; 1969 Dec; 12(4):215-22. PubMed ID: 5309411
[No Abstract] [Full Text] [Related]
6. Brief clinical report: ring-11 chromosome: phenotype-karyotype correlation with deletions of 11q.
Cousineau AJ; Higgins JV; Scott-Emuakpor AB; Mody G
Am J Med Genet; 1983 Jan; 14(1):29-35. PubMed ID: 6829609
[TBL] [Abstract][Full Text] [Related]
7. [Indentification of chromosomal polymorphisms and some aberrations identified by new cytogenetical methods (author's transl)].
Kunze J; Tolksdorf M
Z Kinderheilkd; 1974 Apr; 117(1):29-46. PubMed ID: 4275663
[No Abstract] [Full Text] [Related]
8. [Holt-Oram syndrome with chromosomopathy (author's transl)].
González Espinosa C; Artiles Pérez L; García Báez M; Otero Gómez A; García Miranda JL
An Esp Pediatr; 1982 Jan; 16(1):77-81. PubMed ID: 7081854
[TBL] [Abstract][Full Text] [Related]
9. [Clinical contribution to the crying cat syndrome].
Maaz HJ; Döring M
Z Arztl Fortbild (Jena); 1971 Apr; 65(8):439-41. PubMed ID: 5006545
[No Abstract] [Full Text] [Related]
10. Terminal deletion of the short arm of chromosome 3.
Lizcano-Gil LA; Figuera LE
Genet Couns; 1994; 5(1):35-8. PubMed ID: 8031533
[TBL] [Abstract][Full Text] [Related]
11. Genetic haploinsufficiency as a phenotypic determinant of a deletion 13q syndrome.
Kasyan AG; Benirschke K
Pediatr Dev Pathol; 2005; 8(6):658-65. PubMed ID: 16328665
[TBL] [Abstract][Full Text] [Related]
12. [Partial deletion of the long arm of a group D (13-15) chromosome :Dq-].
Laurent C; Cotton JB; Nivelon A; Freycon MT
Ann Genet; 1967 Mar; 10(1):25-31. PubMed ID: 5300123
[No Abstract] [Full Text] [Related]
13. Deletion of 7q22 and ectrodactyly.
Rivera H; Sanchez-Corona J; Burgos-Fuentes VR; Melendez-Ruiz MJ
Genet Couns; 1991; 2(1):27-31. PubMed ID: 1741973
[TBL] [Abstract][Full Text] [Related]
14. [Wolf-Hirschhorn-syndrome with high urinary level of heparan sulfate (author's transl)].
Lubec G; Scheibenreiter S; Szilvassy J; Ender H
Padiatr Padol; 1982; 17(2):479-83. PubMed ID: 6212898
[No Abstract] [Full Text] [Related]
15. [Symptomatology of the ring chromosomes of the D group. (2 new observations of type 13r)].
Tolksdorf M; Goll U; Wiedemann HR; Pfeiffer RA
Arch Kinderheilkd; 1970; 181(3):282-95. PubMed ID: 5488682
[No Abstract] [Full Text] [Related]
16. [18 ring chromosome. A clinical and cytopathogenetic study (author's transl)].
Carbone LD; Caffarena G; Arslanian A; Cresta E; de Filippi M; Frateschi M
Pathologica; 1978; 70(1009-1010):687-92. PubMed ID: 755240
[No Abstract] [Full Text] [Related]
17. [Monosomy 7qter (author's transl)].
Lambert JC; Mariani R; Donzeau M; Ferrari M; Boutte P; Ayraud N
Arch Fr Pediatr; 1981 Mar; 38(3):177-80. PubMed ID: 7235841
[TBL] [Abstract][Full Text] [Related]
18. [The partial deletion of the long arm of chromosome 18 (syndrome 18Q-). Report of two cases].
Destiné ML; Punnett HH; Thovichit S; DiGeorge AM; Weiss L
Ann Genet; 1967 Jun; 10(2):65-9. PubMed ID: 5298975
[No Abstract] [Full Text] [Related]
19. [Coloboma and anal atresia: phenotype of a chromosome aberration?].
Pfeiffer RA; Heimann K; Heiming E; Schlack H; Maul H
Klin Monbl Augenheilkd; 1971 Sep; 159(3):357-67. PubMed ID: 5003627
[No Abstract] [Full Text] [Related]
20. [12 p trisomy. A new case (author's transl)].
Kubryk N; Prieur M; Borde M
Ann Pediatr (Paris); 1980 Dec; 27(10):695-9. PubMed ID: 7212558
[No Abstract] [Full Text] [Related]
[Next] [New Search]
