Published in Am J Med Genet on May 15, 1993
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A family with three sibs carrying trisomy 21. Ann Genet (1975) 1.02
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Persisting virulence of T. pallidum after incubation with penicillin in Nelson-Mayer medium. Br J Vener Dis (1972) 0.99
The autosomal recessive form of spondylocostal dysostosis. Radiology (1974) 0.98
The Coffin-Siris syndrome in two siblings. Pediatr Radiol (1986) 0.97
Distinctive hair changes (pili torti) in Rapp-Hodgkin ectodermal dysplasia syndrome. Clin Genet (1982) 0.96
Extra band in the 9qh+ chromosome in a normal father and in his child with multiple congenital anomalies. Hum Genet (1982) 0.96
Partial deletion of the short arm of chromosome 20: 46,XX,del(20)(p11)/46,XX mosaicism. Clin Genet (1988) 0.94
Oro-facial-digital syndrome II. Transitional type between the Mohr and the Majewski syndromes: report of two new cases. Clin Genet (1987) 0.94
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Arterial tortuosity syndrome. Am J Med Genet (2000) 0.90
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Interstitial deletion of the long arm of chromosome 2 (q31q33) in a girl with multiple anomalies and mental retardation. Hum Genet (1983) 0.88
In an elite cross of maize a major quantitative trait locus controls one-fourth of the genetic variation for grain yield. Theor Appl Genet (1995) 0.87
Peculiar facial appearance and generalized brachydactyly in a patient with congenital onychodysplasia of the index fingers (Iso-Kikuchi syndrome). Am J Med Genet (2001) 0.87
Psychomotor development in Cri du Chat Syndrome. Clin Genet (2000) 0.86
Long first metacarpal in monozygotic twins with probable Baller-Gerold syndrome. Am J Med Genet (1998) 0.85
Distinctive skeletal dysplasia in Cockayne syndrome. Pediatr Radiol (1986) 0.85
Protective effect of melatonin against hippocampal DNA damage induced by intraperitoneal administration of kainate to rats. Neuroscience (1996) 0.85
Early onset of gastric carcinoma and constitutional deletion of 18p. Cancer Genet Cytogenet (1999) 0.84
Does ethnicity predict lactation? A study of four ethnic communities. Eur J Epidemiol (2001) 0.84
Trends in HIV infection among sexually transmitted disease patients in Paris. AIDS (1996) 0.84
Possible relationship between ulnar-mammary syndrome and split hand with aplasia of the ulna syndrome. Am J Med Genet (1992) 0.84
Patterson-Lowry rhizomelic dysplasia: report of two new patients. Am J Med Genet A (2004) 0.84
Pierre Robin syndrome with hyperphalangism-clinodactylysm of the index finger: a possible new palato-digital syndrome. Pediatr Radiol (1977) 0.83
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Macrocephaly-Cutis marmorata telangiectatica congenita without cutis marmorata? Am J Med Genet (2000) 0.82
Vitamin D at term of pregnancy and during lactation in white and black women living in Northern Italy. Minerva Ginecol (2010) 0.81
HIV-1 seroprevalence in patients presenting with sexually transmitted disease (STD): results from six Parisian STD clinics. AIDS (1991) 0.81
Inguinal hernia and atrial septal defect in Tel Hashomer camptodactyly syndrome: report of a new case expanding the phenotypic spectrum of the disease. Am J Med Genet (1993) 0.81
Duplication of the pituitary stalk in a patient with a heterozygous deletion of chromosome 14 harboring the thyroid transcription factor-1 gene. J Clin Endocrinol Metab (2010) 0.81
Neuroprotective effects of melatonin. Adv Exp Med Biol (1996) 0.80
Blast cell proliferation in perinatal leukaemia with chromosomal translocation(Bq+; Dq-). Helv Paediatr Acta (1972) 0.80
Filippi syndrome: a specific MCA/MR complex within the spectrum of so called "craniodigital syndromes". Report of an additional patient with a peculiar mpp and review of the literature. Genet Couns (2002) 0.80
[Kala-azar in immunosuppressed patients. Apropos of a case disclosed by skin lesions]. Presse Med (1984) 0.80
Radioulnar synostosis and XYY syndrome. Clin Dysmorphol (2000) 0.80
Lower lip pits and complete idiopathic precocious puberty in a patient with Kabuki make-up (Niikawa-Kuroki) syndrome. Am J Med Genet (1993) 0.79
In vitro and in vivo protection against kainate-induced excitotoxicity by melatonin. J Pineal Res (1996) 0.79
Stereotactic radiotherapy for isolated nodal recurrence of prostate cancer. World J Urol (2014) 0.79
The Neu-COFS (cerebro-oculo-facio-skeletal) syndrome: report of a case. Clin Genet (1984) 0.79
Cerebrofaciothoracic dysplasia: a new family. J Med Genet (1992) 0.79
Variability of clinical and immunological phenotype in immunodeficiency-centromeric instability-facial anomalies syndrome. Report of two new patients and review of the literature. Eur J Pediatr (1995) 0.78
Role of radiotherapy boost in women with ductal carcinoma in situ: a single-center experience in a series of 389 patients. Eur J Surg Oncol (2013) 0.78
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[Not Available]. Physis Riv Int Stor Sci (1971) 0.78
Prenatal diagnosis of Nonne-Milroy lymphedema. Ultrasound Obstet Gynecol (2001) 0.77
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Kainic acid induces selective mitochondrial oxidative phosphorylation enzyme dysfunction in cerebellar granule neurons: protective effects of melatonin and GSH ethyl ester. FASEB J (2001) 0.76
Kniest disease with Pierre Robin syndrome and hydrocephalus. Pediatr Radiol (1983) 0.75
Sex chromosome anomalies detection and fluorescence. Acta Paediatr Scand (1973) 0.75
Breastfed newborns are at very low risk of hemorrhagic disease. Acta Paediatr (2001) 0.75
A new type of Ehlers-Danlos syndrome associated with tortuous systemic arteries? Acta Paediatr (2003) 0.75
Modified method of filtering cerebrospinal fluid and aqueous humour for the detection of treponemes. Proof of the persistence of their vitality in rabbits. Br J Vener Dis (1974) 0.75
Melatonin prevents the delayed death of hippocampal neurons induced by enhanced excitatory neurotransmission and the nitridergic pathway. FASEB J (1998) 0.75
In vivo protection against kainate-induced apoptosis by the pineal hormone melatonin: effect of exogenous melatonin and circadian rhythm. Restor Neurol Neurosci (1996) 0.75