Published in Am J Med Genet on January 01, 1988
Internipple distance and internipple index. J Natl Med Assoc (2004) 0.79
Deletion 9p syndrome and malignancy: acquired vs. constitutional aberrations? Am J Med Genet (1992) 0.75
The chromosome constitution of 1000 human spermatozoa. Hum Genet (1983) 2.21
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
Childhood masturbation. Clin Pediatr (Phila) (1993) 1.33
Pregnancy complications in type IV Ehlers-Danlos Syndrome. Lancet (1983) 1.16
Reprint requests. How and why they were made. Am J Dis Child (1989) 0.97
Trigonocephaly and associated minor anomalies in mother and son. J Med Genet (1976) 0.95
A dominantly inherited cytogenetic anomaly: a possible cell division mutant. Hum Genet (1983) 0.94
Gene deletion and duplication effects on phenotype and gamma globulin levels. J Med Genet (1971) 0.90
Partial trisomy 20 confirmed by gene dosage studies. Am J Med Genet (1979) 0.88
Prenatal ultrasonic diagnosis of occipital encephalocele. Am J Obstet Gynecol (1978) 0.84
IgA and partial deletions of chromosome 18. Lancet (1969) 0.84
Kinetochore immunofluorescence in micronuclei: a rapid method for the in situ detection of aneuploidy and chromosome breakage in human fibroblasts. Mutat Res (1988) 0.83
Mosaicism in amniotic fluid cell cultures. Birth Defects Orig Artic Ser (1977) 0.83
Maxillonasal dysplasia (Binder's syndrome). Plast Reconstr Surg (1979) 0.83
Prenatal diagnosis of hypophosphatasia. N Engl J Med (1976) 0.82
Sex chromosome mosaicism not detected at amniocentesis. Prenat Diagn (1990) 0.82
Prenatal diagnosis by fetoscopy with subsequent normal delivery: report of a case. Am J Obstet Gynecol (1976) 0.82
Prenatal diagnosis of hypophosphatasia. Birth Defects Orig Artic Ser (1976) 0.81
The antenatal diagnosis of genetic disease. Am J Obstet Gynecol (1974) 0.80
A de novo case of trisomy 10p: gene dosage studies of hexokinase, inorganic pyrophosphatase and adenosine kinase. Hum Genet (1984) 0.80
Infant outcome following mid-trimester amniocentesis: development and physical status at age six months. Br J Obstet Gynaecol (1985) 0.78
A 'new' syndrome of mental retardation with characteristic facies and brachyphalangy. J Med Genet (1977) 0.78
A possible primidone embryopathy. J Pediatr (1979) 0.78
The association of a lymphoreticular malignancy with an 11q deletion: a coincidence or a cancer susceptibility? Hum Genet (1983) 0.75
Autosomal imbalance with a near-normal phenotype: the small effect of trisomy for the short arm of chromosome 18. Birth Defects Orig Artic Ser (1978) 0.75
Factors distinguishing couples at risk for nondisjunction. Can J Genet Cytol (1984) 0.75
Rhabdomyosarcoma simulating dental abscess. Oral Surg Oral Med Oral Pathol (1988) 0.75
[Dilemma: prenatal diagnosis using amniocentesis]. Infirm Can (1977) 0.75
Prenatal diagnosis of hypophosphatasia. Lancet (1977) 0.75
Letter: Prenatal diagnosis of hypophosphatasia. Lancet (1976) 0.75
Use of fetoscopy. Am J Obstet Gynecol (1978) 0.75
Dilemma. Can Nurse (1976) 0.75
Letter: Confirmation of antenatally detected trisomy-D from saline aborted products of conception. Lancet (1974) 0.75
Arthrogryposis multiplex congenita--prenatal assessment with diagnostic ultrasound and fetoscopy. J Pediatr (1979) 0.75
Familial supernumerary nipples. Am J Med Genet (1988) 0.75
Midtrimester amniocentesis: obstetric outcome and neonatal neurobehavioral status. Am J Obstet Gynecol (1984) 0.75
The natural history of aminopterin-induced embryopathy. Birth Defects Orig Artic Ser (1977) 0.75
Ultrasound and amniotic fluid alpha-fetoprotein in the prenatal diagnosis of spina bifida. Obstet Gynecol (1982) 0.75
The genetics of and associated clinical findings in humero-radial synostosis. Clin Genet (1976) 0.75