• 50 Years Ago in The Journal of Pediatrics: Hand-Foot-Genital Syndrome and Its Multiple Genetic Mechanisms
• A case of Müllerian adenosarcoma of the uterus treated with liposomal doxorubicin
• A case of severe proximal focal femoral deficiency with overlapping phenotypes of Al-Awadi-Raas-Rothschild syndrome and Fuhrmann syndrome
• A Chromosome 7 Pericentric Inversion Defined at Single-Nucleotide Resolution Using Diagnostic Whole Genome Sequencing in a Patient with Hand-Foot-Genital Syndrome
• A missense mutation of HOXA13 underlies hand-foot-genital syndrome in a Chinese family
• A new family with the hand-foot-genital syndrome--a wider spectrum of the hamd-foot-uterus syndrome
• A new multiple malformation syndrome of Müllerian dysgenesis and conductive hearing loss with facial hypoplasia, bilateral forearm deformity, brachydactyly, spinal stenosis and scoliosis
• Acro-renal-mandibular syndrome
• Al-Awadi-Raas-Rothschild (limb/pelvis/uterus-hypoplasia/aplasia) syndrome and WNT7A mutations: genetic homogeneity and nosological delineation
• Amniotic band sequence--a debilitating syndrome
• An unusual manifestation of Hand-Foot-Genital Syndrome: Embryonal Rhabdomyosarcoma - A case report
• Analysis of de novo HOXA13 polyalanine expansions supports replication slippage without repair in their generation
• Biochemical abnormality associated with Smith-Lemli-Opitz syndrome in an infant with features of Rutledge multiple congenital anomaly syndrome confirms that the latter is a variant of the former
• Carcinoma of Unknown Primary Presenting as Peripheral Symmetric Gangrene
• Clinically distinct epigenetic subgroups in Silver-Russell syndrome: the degree of H19 hypomethylation associates with phenotype severity and genital and skeletal anomalies
• Dual genetic diagnoses: Atypical hand-foot-genital syndrome and developmental delay due to de novo mutations in HOXA13 and NRXN1
• Dysmorphologic assessment in 115 Mayer-Rokitansky-Küster-Hauser patients
• Familial deletion of the HOXA gene cluster associated with Hand-Foot-Genital syndrome and phenotypic variability
• Fetal hydrometrocolpos with pre-axial mirror polydactyly as a new variant of McKusick-Kaufman syndrome
• Genetic and phenotypic continuum of HOXA genes: A case with double HOXA9/HOXA13 mutations
• Genetics of the female reproductive ducts
• Hand-Foot-Genital Syndrome
• Hand-foot-genital syndrome - analysis of two cases
• Hand-foot-genital syndrome due to a duplication variant in the GC-rich region of HOXA13
• Hand-foot-genital syndrome with a 7p15 deletion: clinically recognizable syndrome
• Hand-foot-uterus syndrome
• Hand-foot-uterus syndrome (or hand-foot-genital syndrome)
• Hand-foot-uterus-(HFU) syndrome with hypospadias: the hand-foot-genital- (HFG) syndrome
• Heritable aspects of uterine anomalies. I. Three familial aggregates with Müllerian fusion anomalies
• Lacrimoauriculodentodigital syndrome with cleft lip/palate and renal manifestations
• Mayer Rokitansky Kuster Hauser (MRKH) syndrome with absent thumbs and big toes
• McKusick-Kaufman Syndrome
• Molecular basis of the clinical features of Al-Awadi-Raas-Rothschild (limb/pelvis/uterus-hypoplasia/aplasia) syndrome (AARRS) and Fuhrmann syndrome
• Müllerian aplasia with hypoplastic thumbs: Two case reports
• Multifaceted Hoxa13 function in urogenital development underlies the Hand-Foot-Genital Syndrome
• Mutation of HOXA13 in hand-foot-genital syndrome
• Neonatal hydrometrocolpos associated with McKusick Kaufman syndrome
• Persistent Urogenital Sinus: Diagnostic Imaging for Clinical Management. What Does the Radiologist Need to Know?
• Phenotypic spectrum associated with SPECC1L pathogenic variants: new families and critical review of the nosology of Teebi, Opitz GBBB, and Baraitser-Winter syndromes
• Radiographic findings in the hand-foot-uterus syndrome (HFUS)
• Severe Developmental Delay in a Patient with 7p21.1-p14.3 Microdeletion Spanning the TWIST Gene and the HOXA Gene Cluster
• Severe manifestations of hand-foot-genital syndrome associated with a novel HOXA13 mutation
• Sorsby syndrome: a report on further generations of the original family
• Stapes anomaly, Gorlin-Goltz and hand-foot-uterus syndrome as partial aspects of a generalized ectodermal-mesodermal abnormality syndrome with variable expression
• The hand-food-uterus syndrome: a new hereditary disorder characterized by hand and foot dysplasia, dermatoglyphic abnormalities, and partial duplication of the female genital tract
• The hand-foot-genital (hand-foot-uterus) syndrome: family report and update
• The hand-foot-uterus syndrome: a case study
• The hand-foot-uterus syndrome. A report of a case with recessive autosomal inheritance
• The McKusick-Kaufman syndrome: recessively inherited vaginal atresia, hydrometrocolpos, uterovaginal duplications, anorectal anomalies, postaxial polydactyly, and congenital heart disease
• The WNT7A G204S mutation is associated with both Al-Awadi-Raas Rothschild syndrome and Fuhrmann syndrome phenotypes