Are Melnick-Needles syndrome and oto-palato-digital syndrome type II allelic?: Observations in a four-generation kindred

American Journal of Medical Genetics

Volumn 71, Issue 3, 1997, Pages 341-347

  Robertson, S ^a   Gunn, T ^a   Allen, B ^a   Chapman, C ^a   Becroft, D ^a  

^a NATIONAL WOMEN S HOSPITAL   (New Zealand)

Author keywords

Melnick Needles syndrome; Multiple congenital anomalies; Oto palato digital syndrome type II; X linked inheritance

Indexed keywords

ALLELISM; ARTICLE; BONE DYSPLASIA; CLINICAL ARTICLE; CLINICAL FEATURE; FEMALE; HUMAN; HUMAN CELL; HUMAN TISSUE; INFANT; MALE; MELNICK NEEDLES SYNDROME; PHENOTYPE; PRIORITY JOURNAL; SYNDROME DELINEATION; X CHROMOSOME LINKAGE;

ABNORMALITIES, MULTIPLE; ADOLESCENT; ADULT; AGED; ALLELES; CHILD; CLEFT PALATE; CRANIOFACIAL ABNORMALITIES; FEMALE; FINGERS; HEARING LOSS, CONDUCTIVE; HUMANS; INFANT, NEWBORN; MALE; MIDDLE AGED; OSTEOCHONDRODYSPLASIAS; PEDIGREE; PHENOTYPE; SYNDROME; TOES;

EID: 0030811797     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19970822)71:3<341::AID-AJMG16>3.0.CO;2-K     Document Type: Article

References (28)