An epidemiological study of facial clefting in Manitoba.

Mode of inheritance of nonsyndromic cleft lip with or without cleft palate: a reanalysis. Am J Hum Genet (1992) 1.66

Epidemiology of facial clefting. Arch Dis Child (1985) 1.43

An epidemiological and genetic study of facial clefting in France. I. Epidemiology and frequency in relatives. J Med Genet (1982) 1.41

Epidemiological and genetic study in 207 cases of oral clefts in Alsace, north-eastern France. J Med Genet (1991) 1.00

Clustering of malformations in the families of South American oral cleft neonates. J Med Genet (1991) 0.92

Unusual clustering of diseases in a Canadian Old Colony (Chortitza) Mennonite kindred and community. CMAJ (1988) 0.80

Birth prevalence of non-syndromic orofacial clefts in Saudi Arabia and the effects of parental consanguinity. Saudi Med J (2015) 0.75

Congenital heart disease in 56,109 births. Incidence and natural history. Circulation (1971) 5.55

The genetics of cleft lip and cleft palate. Am J Hum Genet (1970) 2.94

Congenital cleft lip. A genetic study of 496 propositi. J Med Genet (1971) 2.04

A genetic study of facial clefting in Northern England. Clin Genet (1976) 1.52

GENETIC STUDY OF CLEFT-LIPS AND CLEFT-PALATES BASED UPON 2,828 JAPANESE CASES. Kyushu J Med Sci (1963) 1.36

Epidemiology of congenital clefts of the lip and palate. Public Health Rep (1963) 1.15

The further epidemiological differentiation of cleft lip and palate: a population study of clefts in King County, Washington, 1956-1965. Teratology (1973) 1.01

Cleft lip and palate in parent and child. Plast Reconstr Surg (1969) 0.98

Incidence of cleft lip and palate in British Columbia Indians. J Med Genet (1969) 0.94

A study of fluctuating dermatoglyphic asymmetry in the sibs and parents of cleft lip propositi. Am J Hum Genet (1977) 0.93

Incidence of selected congenital malformations in Iowa. Am J Epidemiol (1971) 0.92

The further epidemiological differentiation of cleft lip and palate: a population study of celfts in King Country, Washington, 1856-1965. Teratology (1973) 0.86

Cleft lip and cleft palate in New South Wales. Aust Dent J (1974) 0.81

STUDIES IN IRON TRANSPORTATION AND METABOLISM. IV. OBSERVATIONS ON THE ABSORPTION OF IRON FROM THE GASTRO-INTESTINAL TRACT. J Clin Invest (1939) 10.38

STUDIES IN IRON TRANSPORTATION AND METABOLISM. III. THE NORMAL FLUCTUATIONS OF SERUM AND "EASILY SPLIT-OFF" BLOOD IRON IN INDIVIDUAL SUBJECTS. J Clin Invest (1939) 3.29

Primary structure and transcription of an amplified genetic locus: the CUP1 locus of yeast. Proc Natl Acad Sci U S A (1984) 3.28

Expression of the peroxisome proliferator-activated receptor gamma (PPARgamma) in human atherosclerosis and regulation in macrophages by colony stimulating factors and oxidized low density lipoprotein. Proc Natl Acad Sci U S A (1998) 2.93

Down syndrome and recent demographic trends in Manitoba. J Med Genet (1978) 2.34

Severe mental retardation, cataracts, short stature, and primary hypogonadism in two brothers. Am J Med Genet (1978) 2.27

Does uptake of antenatal HIV testing depend on the individual midwife? Cross sectional study. BMJ (1998) 2.27

The occupational overuse syndrome. N Z Med J (1994) 2.03

New mutations associated with resistance not detected following zidovudine monotherapy in pregnancy when used in accordance with British HIV Association guidelines. HIV Med (2008) 1.99

Measurements and simulations of ultralow emittance and ultrashort electron beams in the linac coherent light source. Phys Rev Lett (2009) 1.96

A prospective study to assess the frequency of familial clustering of congenital bicuspid aortic valve. J Am Coll Cardiol (1997) 1.88

Infants' ability to use object kind information for object individuation. Cognition (1999) 1.80

Trimodality therapy for malignant pleural mesothelioma: results from an EORTC phase II multicentre trial. Eur Respir J (2010) 1.74

Renal tubular dysgenesis: a not uncommon autosomal recessive syndrome: a review. Am J Med Genet (1992) 1.63

CDKN2A variants in a population-based sample of Queensland families with melanoma. J Natl Cancer Inst (1999) 1.59

Getting the guidance right: optimizing the quality of the UK national guidelines on sexually transmitted infections and closely related conditions. Int J STD AIDS (2004) 1.57

VACTERL with hydrocephalus: further delineation of the syndrome(s) Am J Med Genet (1989) 1.55

Black grandmothers in multigenerational households: diversity in family structure and parenting involvement in the Woodlawn community. Child Dev (1990) 1.55

Phenotypic correlations in patients with ring chromosome 22. Clin Genet (1977) 1.54

Two children with deletion of the long arm of chromosome 4 with breakpoint at band q33. Clin Genet (1982) 1.49

Simpson-Golabi-Behmel syndrome associated with renal dysplasia and embryonal tumor: localization of the gene to Xqcen-q21. Am J Med Genet (1992) 1.46

Specifications for the development of guidelines on the management of sexually transmitted infections and closely related conditions. Int J STD AIDS (2004) 1.45

A preliminary validation of a family history assessment form to select women at risk for breast or ovarian cancer for referral to a genetics center. Clin Genet (2000) 1.44

Computerised information retrieval services in a teaching hospital. Br Med J (1980) 1.41

Contraception and medical gynaecology for HIV-positive women in a one-stop clinic. Int J STD AIDS (2008) 1.41

Medications prescribed for children. N Z Med J (1993) 1.40

The CUP2 gene product, regulator of yeast metallothionein expression, is a copper-activated DNA-binding protein. Mol Cell Biol (1989) 1.38

Asymmetries in ON and OFF visual pathways of humans revealed using contrast-evoked cortical potentials. Vis Neurosci (1988) 1.34

Craniosynostosis. II. Coronal synostosis: its familial characteristics and associated clinical findings in 109 patients lacking bilateral polysyndactyly or syndactyly. Teratology (1977) 1.33

Craniosynostosis. I. Sagittal synostosis: its genetics and associated clinical findings in 214 patients who lacked involvement of the coronal suture(s). Teratology (1976) 1.33

Counseling problems when twins are discovered at genetic amniocentesis. Clin Genet (1979) 1.28

Family planning in genitourinary medicine: an opportunistic service? Genitourin Med (1995) 1.25

Intracellular metabolites of mercaptopurine in children with lymphoblastic leukaemia: a possible indicator of non-compliance? Br J Cancer (1995) 1.25

Effects of minor groove binding drugs on the interaction of TATA box binding protein and TFIIA with DNA. Biochemistry (1994) 1.24

A reordering of human chromosome 19 long-arm DNA markers and identification of markers flanking the myotonic dystrophy locus. Genomics (1989) 1.24

Antenatal screening for syphilis. Still important in preventing disease. BMJ (1998) 1.23

Specific IgE to isocyanates: a useful diagnostic role in occupational asthma. J Allergy Clin Immunol (1998) 1.21

Reduction in size of the myotonic dystrophy trinucleotide repeat mutation during transmission. Science (1993) 1.20

Neural tube defects in Eastern Ontario and Western Quebec: demography and family data. Am J Med Genet (1984) 1.19

The Coffin-Lowry syndrome. Experience from four centres. Clin Genet (1982) 1.18

Simpson-Golabi-Behmel syndrome: genotype/phenotype analysis of 18 affected males from 7 unrelated families. Am J Med Genet (1996) 1.18

Instant electronic imaging systems are superior to Polaroid at detecting sight-threatening diabetic retinopathy. Diabet Med (1998) 1.17

Willingness of homosexual and bisexual men in London to be screened for human immunodeficiency virus. Br Med J (Clin Res Ed) (1986) 1.16

EORTC Elderly Task Force and Lung Cancer Group and International Society for Geriatric Oncology (SIOG) experts' opinion for the treatment of non-small-cell lung cancer in an elderly population. Ann Oncol (2009) 1.12

Implications of malformations not due to amniotic bands in the amniotic band sequence. Am J Med Genet (1986) 1.11

A cytogenetic survey of 14,069 newborn infants. III. an analysis of the significance and cytologic behavior of the Robertsonian and reciprocal translocations. Cytogenet Cell Genet (1978) 1.11

Linkage analysis of the apolipoprotein C2 gene and myotonic dystrophy on human chromosome 19 reveals linkage disequilibrium in a French-Canadian population. Am J Hum Genet (1989) 1.10

Synchronous mating in yeasts. Methods Cell Biol (1975) 1.10

Developing national outcome standards for the management of gonorrhoea and genital chlamydia in genitourinary medicine clinics. Sex Transm Infect (2004) 1.10

Sweeteners, dyes, and other excipients in vitamin and mineral preparations. Clin Pediatr (Phila) (1996) 1.09

News from the frontline: sexually transmitted infections in teenagers attending a genitourinary clinic in south east London. Sex Transm Infect (2002) 1.09

Routine antenatal HIV testing. Is acceptable to women. BMJ (1999) 1.08

Growth and development in thanatophoric dysplasia. Am J Med Genet (1989) 1.07

Routine testing for HIV at infertility clinics. BMJ (1991) 1.06

Association between clinical complete response and pathological complete response after preoperative chemoradiation in patients with gastroesophageal cancer: analysis in a large cohort. Ann Oncol (2012) 1.05

Monoclonal antibodies raised against covalently crosslinked complexes of human immunodeficiency virus type 1 gp120 and CD4 receptor identify a novel complex-dependent epitope on gp 120. Virology (1995) 1.04

The characteristic physiognomy and tissue specific karyotype distribution in the Pallister-Killian syndrome. Clin Genet (1985) 1.03

Evidence for three tumor suppressor loci on chromosome 9p involved in melanoma development. Cancer Res (2001) 1.03

Global predictions and tests of erythroid regulatory regions. Cold Spring Harb Symp Quant Biol (2003) 1.02

Acute pancreatitis in patients with fulminant hepatic failure. Gut (1973) 1.01

N-Acetylaspartate and DARPP-32 levels decrease in the corpus striatum of Huntington's disease mice. Neuroreport (2000) 1.01

COFS syndrome revisited. Birth Defects Orig Artic Ser (1978) 1.00

Targeted therapies in the treatment of advanced/metastatic NSCLC. Eur J Cancer (2009) 0.99

A prospective randomized trial of methotrexate versus cisplatin in the treatment of recurrent squamous cell carcinoma of the head and neck. Cancer (1983) 0.98

Germline CDKN2A mutations in childhood melanoma. J Natl Cancer Inst (1997) 0.98

Geroderma osteodysplastica. A report of two affected families. Hum Genet (1978) 0.97

Do women with pelvic inflammatory disease receive adequate treatment? Int J STD AIDS (1997) 0.96

Trigonocephaly and associated minor anomalies in mother and son. J Med Genet (1976) 0.95

The Bowen-Conradi syndrome -- a highly lethal autosomal recessive syndrome of microcephaly, micrognathia, low birth weight, and joint deformities. Am J Med Genet (1979) 0.94

VACTERL with hydrocephalus: spontaneous chromosome breakage and rearrangement in a family showing apparent sex-linked recessive inheritance. Am J Med Genet (1993) 0.94

Use of fluorescence in situ hybridization to confirm the interpretation of a balanced complex chromosome rearrangement ascertained through prenatal diagnosis. Am J Med Genet (1993) 0.94

An outbreak of S typhimurium in sheep and its consequences. Vet Rec (1976) 0.93

Artifactual hypertension due to transducer cable malfunction. Anesthesiology (1991) 0.92

Mosaic tetrasomy 21 in a liveborn male infant. Clin Genet (1982) 0.92

Low rate of adequate folic acid supplementation in well-educated women of high socioeconomic status attending a genetics clinic. CMAJ (2001) 0.92

APC I1307K increases risk of transition from polyp to colorectal carcinoma in Ashkenazi Jews. Gastroenterology (2001) 0.92

The prognosis of occupational asthma due to detergent enzymes: clinical, immunological and employment outcomes. Clin Exp Allergy (2006) 0.92

Neglect and visual recognition. Brain (1992) 0.91

Proton magnetic resonance spectroscopy in frontotemporal dementia. J Neurol (2006) 0.90

Is there a fetal gasoline syndrome? Teratology (1979) 0.90

Colostral constituents including immunoglobulins in the first three milkings postpartum. J Dairy Sci (1978) 0.89

Apparent Smith-Lemli-Opitz syndrome in a child with a previously undescribed form of mucolipidosis not involving the neurons. Am J Med Genet (1990) 0.89

Osteogenesis imperfecta type IV: evidence of abnormal triple helical structure of type I collagen. Hum Genet (1986) 0.89

Distribution of Boophilus species ticks in Swaziland. Trop Anim Health Prod (1991) 0.88

Absence of the cerebellar granular layer, mental retardation, tapetoretinal degeneration and progressive glomerulopathy: an autosomal recessive oculo-renal-cerebellar syndrome. Am J Med Genet (1982) 0.88

A novel PHF6 mutation results in enhanced exon skipping and mild Börjeson-Forssman-Lehmann syndrome. J Med Genet (2004) 0.88

Characterization and isolation of a sperm-coating antigen from rabbit seminal plasma with capacity to block fertilization. J Reprod Fertil (1969) 0.88

Nuclear and mitochondrial DNA replication during zygote formation and maturation in yeast. Science (1976) 0.88

Effects of diet and time on blood serum proteins in the newborn calf. J Dairy Sci (1970) 0.87

Selective hepatic arterial embolization of grade IV and V blunt hepatic injuries: an extension of resuscitation in the nonoperative management of traumatic hepatic injuries. J Trauma (1998) 0.87

Mutation of the transforming growth factor-beta type II receptor gene in right-sided colorectal cancer: relationship to clinicopathological features and genetic alterations. J Pathol (1998) 0.86

Seminal antigens: their alteration in the genital tract of female rabbits and during partial in vitro capacitation with beta amylase and beta glucuronidase. Biol Reprod (1972) 0.86

CDKN2A is not the principal target of deletions on the short arm of chromosome 9 in neuroendocrine (Merkel cell) carcinoma of the skin. Int J Cancer (2001) 0.86

The use of fibrin glue in intracranial procedures: preliminary results. Laryngoscope (1990) 0.86

Hepatic fibrosis, polycystic kidney, colobomata and encephalopathy in siblings. Clin Genet (1974) 0.86

Interstitial deletion of the long arm of chromosome 10. Ann Genet (1980) 0.85

AvaII RFLP at the human apolipoprotein CII (APO CII) gene locus. Nucleic Acids Res (1987) 0.85

Inheritance of branchial sinuses and preauricular fistulae. Teratology (1974) 0.85

Stress- and endotoxin-induced increases in brain tryptophan and serotonin metabolism depend on sympathetic nervous system activity. J Neurochem (1991) 0.85

Head circumference and intellectual performance of patients with Duchenne muscular dystrophy. Dev Med Child Neurol (1991) 0.85