142 related articles for article (PubMed ID: 6823976)
1. 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]
2. 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]
3. Terminal deletion of (1)(q42) and its phenotypical manifestations.
Andrle M; Erlach A; Mayr WR; Rett A
Hum Genet; 1978 Feb; 41(1):115-20. PubMed ID: 631857
[TBL] [Abstract][Full Text] [Related]
4. De novo 3q/7q translocation and associated interstitial 7q35 deletion.
Fryns JP; Kleczkowska A; van den Berghe H
Clin Genet; 1988 Jan; 33(1):60-2. PubMed ID: 3342549
[TBL] [Abstract][Full Text] [Related]
5. Reproductive failure in a carrier of inv dupl l(q21.4----q12).
Toncheva D; Genkova P; Tzoneva M; Lozanova T; Angelova E; Mitreva B
Acta Paediatr Hung; 1986; 27(1):61-6. PubMed ID: 3730184
[TBL] [Abstract][Full Text] [Related]
6. Interstitial deletion of the long arm of chromosome 2 (q31q33) in a girl with multiple anomalies and mental retardation.
Franceschini P; Cirillo Silengo M; Davi G; Bianco R; Biagioli M
Hum Genet; 1983; 64(1):98. PubMed ID: 6873945
[No Abstract] [Full Text] [Related]
7. Inverted tandem duplication generates a duplication deficiency of chromosome 8p.
Dill FJ; Schertzer M; Sandercock J; Tischler B; Wood S
Clin Genet; 1987 Aug; 32(2):109-13. PubMed ID: 2888552
[TBL] [Abstract][Full Text] [Related]
8. Monosomy 1pter.
Yunis E; Quintero L; Leibovici M
Hum Genet; 1981; 56(3):279-82. PubMed ID: 7239511
[No Abstract] [Full Text] [Related]
9. 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]
10. Partial deletion of 1q, following a pericentric inversion, in a boy with multiple minor morphologic anomalies and mental retardation.
Schwanitz G; Schmid P; Hägele C; Daffner HW; Grosse KP
Acta Genet Med Gemellol (Roma); 1977; 26(2):173-5. PubMed ID: 596113
[TBL] [Abstract][Full Text] [Related]
11. A specific syndrome due to deletion of the distal long arm of chromosome 1.
Meinecke P; Vögtel D
Am J Med Genet; 1987 Oct; 28(2):371-6. PubMed ID: 3322005
[TBL] [Abstract][Full Text] [Related]
12. Partial monosomy of long arm of chromosome 4 due to interstitial deletion.
McDermott A; Cain R; Howell R
Hum Genet; 1980; 53(3):305-7. PubMed ID: 7372333
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Interstitial deletion of the long arm of chromosome 3 in a patient with mental retardation and congenital anomalies.
Franceschini P; Cirillo Silengo M; Davi G; Bianco R; Biagioli M
Hum Genet; 1983; 64(1):97. PubMed ID: 6873944
[No Abstract] [Full Text] [Related]
15. 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]
16. Multiple congenital anomalies/mental retardation (MCA/MR) syndrome due to interstitial deletion 1q.
Steinbach P; Wolf M; Schmidt H
Am J Med Genet; 1984 Sep; 19(1):131-6. PubMed ID: 6496565
[TBL] [Abstract][Full Text] [Related]
17. Mild phenotypic manifestations of terminal deletion of the long arm of chromosome 4: clinical description of a new patient.
Caliebe A; Waltz S; Jenderny J
Clin Genet; 1997 Aug; 52(2):116-9. PubMed ID: 9298747
[TBL] [Abstract][Full Text] [Related]
18. Monosomy, trisomy, fragile sites, and rearrangements of chromosome no. 1 in a mentally retarded male with multiple congenital anomalies.
Neu RL; Kousseff BG; Madan S; Essig YP; Miller K; Tedesco TA
Clin Genet; 1988 Feb; 33(2):73-7. PubMed ID: 3359669
[TBL] [Abstract][Full Text] [Related]
19. Additional case of de novo interstitial deletion del(17)(q21.3q23) and expansion of the phenotype.
Khalifa MM; MacLeod PM; Duncan AM
Clin Genet; 1993 Nov; 44(5):258-61. PubMed ID: 7906212
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
