Indexed keywords
ESTROGEN;
ORAL CONTRACEPTIVE AGENT;
ADULT;
AGENESIS;
ARTICLE;
CHROMOSOME ANALYSIS;
CLINICAL FEATURE;
CLINICAL TRIAL;
CONGENITAL BLOOD VESSEL MALFORMATION;
COUNSELING;
CUTIS MARMORATA TELANGIECTATICA CONGENITA;
DOPPLER FLOWMETER;
ECHOGRAPHY;
EMBRYO TRANSFER;
ESTROGEN DEFICIENCY;
FEMALE;
FERTILIZATION IN VITRO;
FOLLITROPIN BLOOD LEVEL;
HORMONE SUBSTITUTION;
HUMAN;
HYSTEROSCOPY;
LABORATORY TEST;
MENOPAUSE;
MENSTRUATION;
NUCLEAR MAGNETIC RESONANCE IMAGING;
OOCYTE;
OVARY INSUFFICIENCY;
PHENOTYPE;
PIGMENTATION;
PRIORITY JOURNAL;
RECIPROCAL CHROMOSOME TRANSLOCATION;
REPRODUCTIVE PROCEDURES;
SKIN DEFECT;
SPECULAR MICROSCOPY;
TREATMENT OUTCOME;
VARICOSIS;
ABNORMALITIES, MULTIPLE;
ADULT;
CHROMOSOMES, HUMAN, PAIR 8;
CHROMOSOMES, HUMAN, PAIR 9;
FEMALE;
HUMANS;
OVARIAN FAILURE, PREMATURE;
OVARY;
SKIN DISEASES, VASCULAR;
TELANGIECTASIS;
TRANSLOCATION, GENETIC;
UTERUS;
1
0033849079
Cutis marmorata telangiectatica congenita: Clinical findings in 85 patients
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Lapidoth, M.5
Metzker, A.6
2
0040288557
X-chromosome abnormalities in women with premature ovarian failure
Devi A., Eenn P.A. X-chromosome abnormalities in women with premature ovarian failure. J Reprod Med. 44:1999;321-324.
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J Reprod Med
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Autoimmunity in a patient with 47,XXX karyotype
Michalak D.P., Zacur H.A., Rock J.A., Woodruff J.D. Autoimmunity in a patient with 47,XXX karyotype. Obstet Gynecol. 62:1983;667-669.
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Obstet Gynecol
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Michalak, D.P.1
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Woodruff, J.D.4
4
0020564712
Triple-X syndrome and premature ovarian failure
Villanueva A.L., Rebar R.W. Triple-X syndrome and premature ovarian failure. Obstet Gynecol. 62:(Suppl 3):1983;70s-73s.
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Obstet Gynecol
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Villanueva, A.L.1
Rebar, R.W.2
5
0026954074
True 47,XXX in a patient with premature ovarian failure: The first reported case in Thailand
Tungphaisal S., Jinorose U. True 47,XXX in a patient with premature ovarian failure the first reported case in Thailand . J Med Assoc Thai. 75:1992;661-665.
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X-chromosome abnormalities in women with premature ovarian failure
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Eenn, P.A.2
7
0033762922
Molecular definition of Xq common-deleted region in patients affected by premature ovarian failure
Marozzi A., Manfredini E., Tibiletti M.G., Furlan D., Villa N., Vegetti W., et al. Molecular definition of Xq common-deleted region in patients affected by premature ovarian failure. Hum Genet. 107:2000;304-311.
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Tibiletti, M.G.3
Furlan, D.4
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Vegetti, W.6
8
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Premature ovarian failure due to an unbalanced translocation on the X chromosome
Ashraf M., Jayawickrama N.S., Bowen-Simpkins P. Premature ovarian failure due to an unbalanced translocation on the X chromosome. Br J Obstet Gynaecol. 108:2001;230-232.
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Ashraf, M.1
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9
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47,XXY in an adolescent with premature ovarian failure and autoimmune disease
Holland C.M. 47,XXY in an adolescent with premature ovarian failure and autoimmune disease. J Pediatr Adolesc Gynecol. 14:2001;77-80.
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Holland, C.M.1
10
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Balanced autosomal translocation and ovarian dysgenesis
Tupler R., Barbierato L., Larizza D., Sampaolo P., Piovella F., Maraschio P. Balanced autosomal translocation and ovarian dysgenesis. Hum Genet. 94:1994;171-176.
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Tupler, R.1
Barbierato, L.2
Larizza, D.3
Sampaolo, P.4
Piovella, F.5
Maraschio, P.6
11
0029019887
Gonadal dysenesis in del(18p) syndrome
Telvi L., Bernheim A., Ion A., Fouquet F., Le Bouc Y., Chaussain J.L. Gonadal dysenesis in del(18p) syndrome. Am J Med Genet. 57:1995;598-600.
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Telvi, L.1
Bernheim, A.2
Ion, A.3
Fouquet, F.4
Le Bouc, Y.5
Chaussain, J.L.6
13
0018651807
Cutis marmorata telangiectatica congenita in two sisters
Andreev J.C., Pramatarov K. Cutis marmorata telangiectatica congenita in two sisters. Br J Dermatol. 10:1979;345-350.
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Pramatarov, K.2
14
0019943575
Hereditary cutis marmorata telangiectatica congenita
Kurczynski T.W. Hereditary cutis marmorata telangiectatica congenita. Pediatrics. 70:1982;52-53.
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Kurczynski, T.W.1