142 related articles for article (PubMed ID: 937003)
1. Primary hypothyroidism, growth hormone deficiency and congenital malformations in a child with the karyotype 46,XY,del(1)(q25q32).
Koivisto M; Akerblom HK; Remes M; de La Chapelle A
Acta Paediatr Scand; 1976 Jul; 65(4):513-8. PubMed ID: 937003
[TBL] [Abstract][Full Text] [Related]
2. Two cases of interstitial deletion of the long arm of chromosome 1: del(1)(q21----q25) and del(1)(q41----q43).
Beemer FA; Klep-de Pater JM; Sepers GJ; Janssen B
Clin Genet; 1985 May; 27(5):515-9. PubMed ID: 4006278
[TBL] [Abstract][Full Text] [Related]
3. Interstitial deletion in the long arms of chromosome 1: 46,XY,del(1)(pter leads to q22::q25 leads to qter).
de Pablo CE; García Sagredo JM; Ferro MT; Ferrando P; San Román C
J Med Genet; 1980 Dec; 17(6):483-6. PubMed ID: 6937620
[TBL] [Abstract][Full Text] [Related]
4. Jacobsen syndrome: report of a patient with severe eye anomalies, growth hormone deficiency, and hypothyroidism associated with deletion 11 (q23q25) and review of 52 cases.
Pivnick EK; Velagaleti GV; Wilroy RS; Smith ME; Rose SR; Tipton RE; Tharapel AT
J Med Genet; 1996 Sep; 33(9):772-8. PubMed ID: 8880580
[TBL] [Abstract][Full Text] [Related]
5. The phenotype of ring chromosome 3.
Wilson GN; Pooley J; Parker J
J Med Genet; 1982 Dec; 19(6):471-3. PubMed ID: 7154048
[TBL] [Abstract][Full Text] [Related]
6. Interstitial deletion of the long arm of chromosome 5 in a deformed boy: 46,XY,del(5)(q13q15).
Stoll C; Levy J; Roth MP
J Med Genet; 1980 Dec; 17(6):486-7. PubMed ID: 7205434
[TBL] [Abstract][Full Text] [Related]
7. A case of 46,XY,t(1;13) (q24;q32) with mental retardation.
Wilbur L; Curcuru-Giordano FM; Krishna SG; Kardon NB; Jenkins EC
Hum Genet; 1977 Jun; 37(2):239-42. PubMed ID: 885541
[TBL] [Abstract][Full Text] [Related]
8. De novo interstitial deletion of the long arm of chromosome 2 in a malformed newborn with a karyotype: 46,XY,del(2)(q12q14).
Antich J; Carbonell X; Mas J; Clusellas N
Acta Paediatr Scand; 1983 Jul; 72(4):631-3. PubMed ID: 6624439
[TBL] [Abstract][Full Text] [Related]
9. Terminal deletion with stable acentric fragment of 1q in a child with congenital malformations.
Kucerová M; Polívková Z; Dluholucký S; Kvasnicová M
Am J Hum Genet; 1983 Jan; 35(1):91-5. PubMed ID: 6823976
[TBL] [Abstract][Full Text] [Related]
10. Interstitial deletion of chromosome 1 (q23-q25). Report of a case.
Silengo MC; Davi GF; Bianco R; Biagioli M; Guala A; Franceschini P; Novelli G
Clin Genet; 1984 Jun; 25(6):549-52. PubMed ID: 6587954
[TBL] [Abstract][Full Text] [Related]
11. Absence of constitutive heterochromatin in a partially identified supernumerary marker chromosome.
Pai GS; Thomas GH; Benke PJ
J Med Genet; 1981 Oct; 18(5):392-4. PubMed ID: 6948963
[TBL] [Abstract][Full Text] [Related]
12. A case of interstitial 1q deletion [46,XY,del(q25q32.1)].
Hamano S; Fukushima Y; Yamada T; Shimizu H; Okuyama M; Ito F; Maekawa K
Ann Genet; 1987; 30(2):105-8. PubMed ID: 3314663
[TBL] [Abstract][Full Text] [Related]
13. [Phenotypic and genetic analysis of a boy with 3p26.3-pter deletion and 7q31.33-qter duplication].
Feng L; Cai W; Jiang J; Sun S; Jing C; Yuan L
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Aug; 35(4):535-539. PubMed ID: 30098251
[TBL] [Abstract][Full Text] [Related]
14. Interstitial deletion of chromosome 13: prognosis and adult phenotype.
Dean JC; Simpson S; Couzin DA; Stephen GS
J Med Genet; 1991 Aug; 28(8):533-5. PubMed ID: 1920369
[TBL] [Abstract][Full Text] [Related]
15. Centric fission of chromosome 7 with 47,XX,del(7)(pter----cen::q21----qter)+cen fr karyotype in a mother and proximal 7q deletion in two malformed newborns.
Fryns JP; Kleczkowska A; Limbos C; Vandecasseye W; Van den Berghe H
Ann Genet; 1985; 28(4):248-50. PubMed ID: 3879440
[TBL] [Abstract][Full Text] [Related]
16. Two cases with different deletions of the long arm of chromosome 7.
Klep-de Pater JM; Bijlsma JB; Bleeker-Wagemakers EM; de France HF; de Vries-Ekkers CM
J Med Genet; 1979 Apr; 16(2):151-4. PubMed ID: 458833
[TBL] [Abstract][Full Text] [Related]
17. De novo interstitial deletion del(1)(p21p32).
Bene M; Duca-Marinescu A; Ioan D; Maximilian C
J Med Genet; 1979 Aug; 16(4):323-7. PubMed ID: 490590
[TBL] [Abstract][Full Text] [Related]
18. Terminal long-arm deletion of chromosome 1 in a male infant.
Dignan PS; Soukup S
Hum Genet; 1979 Apr; 48(2):151-6. PubMed ID: 457139
[TBL] [Abstract][Full Text] [Related]
19. A girl with karyotype 46,XX,del(7)(pter leads to q32:).
Friedrich U; Osterballe O; Stenbjerg S; Jørgensen J
Hum Genet; 1979 Oct; 51(2):231-5. PubMed ID: 511152
[No Abstract] [Full Text] [Related]
20. Two cases of interstitial deletion 1p.
Lai MM; Robards MF; Berry AC; Fear CN; Hart C
J Med Genet; 1991 Feb; 28(2):128-30. PubMed ID: 2002484
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
