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Mental retardation, microbrachycephaly, hypotelorism, palpebral ptosis, thin/long face, cleft lip, and lumbosacral/pelvic anomalies.
Am J Med Genet. 1992 Jun 01; 43(3):565-8.AJ

Abstract

We describe 2 Brazilian sisters with a combination of clinical signs strongly suggesting a new autosomal recessive MCA/MR syndrome.

Authors+Show Affiliations

Serviço de Genética Clínica, Hospital de Pesquisa e Reabilitação de Lesões Lábio-Palatais, Universidade de São Paulo, Brazil.No affiliation info availableNo affiliation info available

Pub Type(s)

Case Reports
Journal Article

Language

eng

PubMed ID

1605250

Citation

Richieri-Costa, A, et al. "Mental Retardation, Microbrachycephaly, Hypotelorism, Palpebral Ptosis, Thin/long Face, Cleft Lip, and Lumbosacral/pelvic Anomalies." American Journal of Medical Genetics, vol. 43, no. 3, 1992, pp. 565-8.
Richieri-Costa A, Guion-Almeida ML, Ramos AL. Mental retardation, microbrachycephaly, hypotelorism, palpebral ptosis, thin/long face, cleft lip, and lumbosacral/pelvic anomalies. Am J Med Genet. 1992;43(3):565-8.
Richieri-Costa, A., Guion-Almeida, M. L., & Ramos, A. L. (1992). Mental retardation, microbrachycephaly, hypotelorism, palpebral ptosis, thin/long face, cleft lip, and lumbosacral/pelvic anomalies. American Journal of Medical Genetics, 43(3), 565-8.
Richieri-Costa A, Guion-Almeida ML, Ramos AL. Mental Retardation, Microbrachycephaly, Hypotelorism, Palpebral Ptosis, Thin/long Face, Cleft Lip, and Lumbosacral/pelvic Anomalies. Am J Med Genet. 1992 Jun 1;43(3):565-8. PubMed PMID: 1605250.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Mental retardation, microbrachycephaly, hypotelorism, palpebral ptosis, thin/long face, cleft lip, and lumbosacral/pelvic anomalies. AU - Richieri-Costa,A, AU - Guion-Almeida,M L, AU - Ramos,A L, PY - 1992/6/1/pubmed PY - 1992/6/1/medline PY - 1992/6/1/entrez SP - 565 EP - 8 JF - American journal of medical genetics JO - Am J Med Genet VL - 43 IS - 3 N2 - We describe 2 Brazilian sisters with a combination of clinical signs strongly suggesting a new autosomal recessive MCA/MR syndrome. SN - 0148-7299 UR - https://www.unboundmedicine.com/medline/citation/1605250/Mental_retardation_microbrachycephaly_hypotelorism_palpebral_ptosis_thin/long_face_cleft_lip_and_lumbosacral/pelvic_anomalies_ L2 - https://onlinelibrary.wiley.com/resolve/openurl?genre=article&sid=nlm:pubmed&issn=0148-7299&date=1992&volume=43&issue=3&spage=565 DB - PRIME DP - Unbound Medicine ER -