175 related articles for article (PubMed ID: 7957420)
1. Molecular study of human growth hormone gene cluster in three families with isolated growth hormone deficiency and similar phenotype.
Cacciari E; Pirazzoli P; Gualandi S; Baroncini C; Baldazzi L; Trevisani B; Capelli M; Zucchini S; Balsamo A; Cicognani A
Eur J Pediatr; 1994 Sep; 153(9):635-41. PubMed ID: 7957420
[TBL] [Abstract][Full Text] [Related]
2. Isolated growth hormone (GH) deficiency type 1A associated with a double deletion in the human GH gene cluster.
Goossens M; Brauner R; Czernichow P; Duquesnoy P; Rappaport R
J Clin Endocrinol Metab; 1986 Apr; 62(4):712-6. PubMed ID: 3005356
[TBL] [Abstract][Full Text] [Related]
3. Prevalence of human growth hormone-1 gene deletions among patients with isolated growth hormone deficiency from different populations.
Mullis PE; Akinci A; Kanaka C; Eblé A; Brook CG
Pediatr Res; 1992 May; 31(5):532-4. PubMed ID: 1603635
[TBL] [Abstract][Full Text] [Related]
4. Isolated growth hormone deficiency: analysis of the growth hormone (GH)-releasing hormone gene and the GH gene cluster.
Mullis P; Patel M; Brickell PM; Brook CG
J Clin Endocrinol Metab; 1990 Jan; 70(1):187-91. PubMed ID: 1967179
[TBL] [Abstract][Full Text] [Related]
5. Genetic and molecular analysis of familial isolated growth hormone deficiency.
Ruiz-Pacheco R; Chatelain P; Sizonenko PC; Bost M; Garandau P; Sultan C
Hum Genet; 1993 Oct; 92(3):273-81. PubMed ID: 8104861
[TBL] [Abstract][Full Text] [Related]
6. Isolated growth hormone deficiency type IA associated with a 45-kilobase gene deletion within the human growth hormone gene cluster in an Italian family.
Ghizzoni L; Duquesnoy P; Torresani T; Vottero A; Goossens M; Bernasconi S
Pediatr Res; 1994 Nov; 36(5):654-9. PubMed ID: 7877887
[TBL] [Abstract][Full Text] [Related]
7. Isolated growth hormone (GH) deficiency type IA associated with a 45-kilobase gene deletion within the human GH gene cluster.
Akinci A; Kanaka C; Eblé A; Akar N; Vidinlisan S; Mullis PE
J Clin Endocrinol Metab; 1992 Aug; 75(2):437-41. PubMed ID: 1322425
[TBL] [Abstract][Full Text] [Related]
8. [hGH and molecular biology].
Goossens M
Ann Endocrinol (Paris); 1986; 47(5):363-71. PubMed ID: 3548571
[TBL] [Abstract][Full Text] [Related]
9. Molecular examination of GH gene deletion in familial growth hormone deficiency.
Lekhakula S; Lertrit P; Tuchinda C; Angsusingha K; Kangsadalampai S; Wacharasindhu S; Futrakul A; Sritawil K
Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():207-11. PubMed ID: 8629108
[TBL] [Abstract][Full Text] [Related]
10. Reduced human growth hormone (hGH) bioactivity without a defect of the GH-1 gene in three patients with rhGH responsive growth failure.
Binder G; Benz MR; Elmlinger M; Pflaum CD; Strasburger CJ; Ranke MB
Clin Endocrinol (Oxf); 1999 Jul; 51(1):89-95. PubMed ID: 10468970
[TBL] [Abstract][Full Text] [Related]
11. Isolated human growth hormone deficiency due to the hGH-I gene deletion with (type IA) and without (the Israeli-type) hGH antibody formation during hGH therapy.
Nishi Y; Masuda H; Nishimura S; Kihara M; Suwa S; Tachibana K; Takeda M; Okada Y; Matsuda I
Acta Endocrinol (Copenh); 1990 Feb; 122(2):267-71. PubMed ID: 1969217
[TBL] [Abstract][Full Text] [Related]
12. Human growth hormone gene deletion without antibody formation or growth arrest during treatment--a new disease entity?
Laron Z; Kelijman M; Pertzelan A; Keret R; Shoffner JM; Parks JS
Isr J Med Sci; 1985 Dec; 21(12):999-1006. PubMed ID: 3005192
[TBL] [Abstract][Full Text] [Related]
13. The human growth hormone gene locus: structure, evolution, and allelic variations.
Hirt H; Kimelman J; Birnbaum MJ; Chen EY; Seeburg PH; Eberhardt NL; Barta A
DNA; 1987 Feb; 6(1):59-70. PubMed ID: 3030680
[TBL] [Abstract][Full Text] [Related]
14. Phenotypic heterogeneity in familial isolated growth hormone deficiency type I-A.
Rivarola MA; Phillips JA; Migeon CJ; Heinrich JJ; Hjelle BJ
J Clin Endocrinol Metab; 1984 Jul; 59(1):34-40. PubMed ID: 6327759
[TBL] [Abstract][Full Text] [Related]
15. Detection of placental growth hormone variant and chorionic somatomammotropin ribonucleic acid expression in human trophoblastic neoplasms by reverse transcriptase-polymerase chain reaction.
Lytras A; Bock ME; Dodd JG; Cattini PA
Endocrinology; 1994 Jun; 134(6):2461-7. PubMed ID: 7515000
[TBL] [Abstract][Full Text] [Related]
16. Constitutionally short stature: analysis of the insulin-like growth factor-I gene and the human growth hormone gene cluster.
Mullis PE; Patel MS; Brickell PM; Brook CG
Pediatr Res; 1991 Apr; 29(4 Pt 1):412-5. PubMed ID: 1677176
[TBL] [Abstract][Full Text] [Related]
17. A gene deletion is responsible for absence of human chorionic somatomammotropin.
Wurzel JM; Parks JS; Herd JE; Nielsen PV
DNA; 1982; 1(3):251-7. PubMed ID: 7169010
[TBL] [Abstract][Full Text] [Related]
18. The use of the polymerase chain reaction in prenatal diagnosis of growth hormone gene deletions.
Mullis PE; Brickell PM
Clin Endocrinol (Oxf); 1992 Jul; 37(1):89-95. PubMed ID: 1424197
[TBL] [Abstract][Full Text] [Related]
19. Splicing variants of the human growth hormone mRNA: detection in pituitary, mononuclear cells and dermal fibroblasts.
Palmetshofer A; Zechner D; Luger TA; Barta A
Mol Cell Endocrinol; 1995 Sep; 113(2):225-34. PubMed ID: 8674830
[TBL] [Abstract][Full Text] [Related]
20. Screening for growth hormone (GH) gene splice-site mutations in sporadic cases with severe isolated GH deficiency using ectopic transcript analysis.
Binder G; Ranke MB
J Clin Endocrinol Metab; 1995 Apr; 80(4):1247-52. PubMed ID: 7714096
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
